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nsv6430795

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,672

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 18 studies. See in: genome view    
    Submitted genomic38,116,164-38,119,835Question Mark
    Overlapping variant regions from other studies: 145 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):37,973,682-37,977,353Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6430795Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr838,116,16438,119,835
    nsv6430795RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr837,973,68237,977,353

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18168931deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18168931Submitted genomicNC_000008.11:g.381
    16164_38119835del
    GRCh38 (hg38)NC_000008.11Chr838,116,16438,119,835
    nssv18168931RemappedPerfectNC_000008.10:g.379
    73682_37977353del
    GRCh37.p13First PassNC_000008.10Chr837,973,68237,977,353

    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)
    nssv18168931<0.001139082
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