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nsv6373666

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,196

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
    Submitted genomic57,231,754-57,232,949Question Mark
    Overlapping variant regions from other studies: 83 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):57,265,782-57,266,977Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6373666Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr357,231,75457,232,949
    nsv6373666RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr357,265,78257,266,977

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18103498deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18103498Submitted genomicNC_000003.12:g.572
    31754_57232949del
    GRCh38 (hg38)NC_000003.12Chr357,231,75457,232,949
    nssv18103498RemappedPerfectNC_000003.11:g.572
    65782_57266977del
    GRCh37.p13First PassNC_000003.11Chr357,265,78257,266,977

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18103498<0.001138340
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