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nsv6773467

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,150

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 22 studies. See in: genome view    
    Submitted genomic76,461,144-76,472,293Question Mark
    Overlapping variant regions from other studies: 103 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):75,756,969-75,768,118Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6773467Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr576,461,14476,472,293
    nsv6773467RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr575,756,96975,768,118

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18516407deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18516407Submitted genomicNC_000005.10:g.764
    61144_76472293del
    GRCh38 (hg38)NC_000005.10Chr576,461,14476,472,293
    nssv18516407RemappedPerfectNC_000005.9:g.7575
    6969_75768118del
    GRCh37.p13First PassNC_000005.9Chr575,756,96975,768,118

    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)
    nssv185164074e-061276258
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