This is a demonstration environment. It may contain non-accurate test data and should not be used for real-world applications. Data will be deleted regularly.
Display Name: Pakistan/LOC_0019PEY.1/2023-07-03
M. Umair, S. A. Haider, Z. Jamal, M. Ammar, R. Hakim, Q. Ali & M. Salman

Sample details

Collection date
2023-07-03
Collection date (lower bound)
2023-07-03
Collection date (upper bound)
2023-07-03
Earliest release date
2023-12-26
Collection country
Pakistan
Isolate name
CCHF/NIHPAK-96/2023

Data use terms

Data use terms
OPEN
Data use terms URL

Authors

Author affiliations
National Institute of Health, Department of Virology

INSDC

NCBI release date
2023-12-26
INSDC accession L
INSDC accession M
INSDC accession S

Host

Host taxon id
Host name scientific
Homo sapiens

Alignment and QC metrics L

Length L
12147
Total SNPs L
1658
Total inserted nucs L
52
Total deleted nucs L
1
Total ambiguous nucs L
0
Total unknown nucs L
0
Total frame shifts L
0
Completeness L
99.90%
Total stop codons L
0

Alignment and QC metrics M

Length M
5334
Total SNPs M
31
Total inserted nucs M
1
Total deleted nucs M
0
Total ambiguous nucs M
0
Total unknown nucs M
49
Total frame shifts M
0
Completeness M
96.83%
Total stop codons M
0

Alignment and QC metrics S

Length S
1651
Total SNPs S
216
Total inserted nucs S
3
Total deleted nucs S
0
Total ambiguous nucs S
0
Total unknown nucs S
0
Total frame shifts S
0
Completeness S
91.25%
Total stop codons S
0

Submission details

Submission ID
OR964922.1.L/OR964933.1.M/OR964911.1.S
Date submitted
2026-01-30 16:05:53 UTC
Date released
2026-01-30 16:09:58 UTC

Files

Nucleotide mutations

Mutations called relative to the NC_005301.3, MH396653.1 & OL774851.1 references

Substitutions

L

  • L:G23T
  • L:G32A
  • L:A35G
  • L:G43T
  • L:T49C
  • L:C63G
  • L:C64T
  • L:T65C
  • L:T66C
  • L:T68C
  • L:G69A
  • L:G71T
  • L:C85T
  • L:G88A
  • L:G93A
  • L:A109G
  • L:C117A
  • L:A124G
  • M

  • M:G433A
  • M:T503C
  • M:T578A
  • M:G602A
  • M:G634A
  • M:T707C
  • M:C720T
  • M:A784G
  • M:A793G
  • M:T804C
  • M:C817T
  • M:T1000C
  • M:A1130G
  • M:A1318G
  • M:A1382G
  • M:T1399C
  • M:A2005T
  • M:A2634G
  • S

  • S:T16A
  • S:C31G
  • S:T63C
  • S:A65G
  • S:A84G
  • S:A93G
  • S:A98T
  • S:A102G
  • S:C123T
  • S:C150T
  • S:G153A
  • S:T156C
  • S:T166C
  • S:A173G
  • S:G174A
  • S:G180A
  • S:A186G
  • S:C192T
  • Deletions
    L:12034
    Insertions
    ins_L:58:T, ins_L:11917:CA, ins_L:12055:ACAATTTC, ins_L:12083:ACTATTC, ins_L:12108:TTTATTATTTCTGGGGTGTGGGGGGAACGATTTC, ins_M:5215:N, ins_S:0:CGT

    Amino acid mutations

    Mutations called relative to the NC_005301.3, MH396653.1 & OL774851.1 references

    Substitutions

    GPC

  • GPC:S139P
  • GPC:S164T
  • GPC:A172T
  • GPC:S207P
  • GPC:S211L
  • GPC:I232M
  • GPC:I239T
  • GPC:T348A
  • GPC:I432V
  • GPC:E849G
  • GPC:I1279V
  • NP

  • NP:N9S
  • NP:Y20F
  • NP:K45R
  • NP:V83A
  • NP:D116E
  • NP:A124S
  • NP:Q179L
  • NP:D199E
  • NP:R270K
  • NP:A307V
  • NP:E322D
  • NP:Q405L
  • RdRp

  • RdRp:S6N
  • RdRp:A14D
  • RdRp:S19T
  • RdRp:Y60N
  • RdRp:R63H
  • RdRp:S67V
  • RdRp:R80K
  • RdRp:V82I
  • RdRp:I114V
  • RdRp:T163A
  • RdRp:A168T
  • RdRp:M172V
  • RdRp:R174K
  • RdRp:S205P
  • RdRp:N206Y
  • RdRp:I223V
  • RdRp:N236S
  • RdRp:K275R
  • Deletions
    None
    Insertions
    None

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