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nsv6791003

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:339

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 116 SVs from 18 studies. See in: genome view    
    Submitted genomic13,307,593-13,307,931Question Mark
    Overlapping variant regions from other studies: 116 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):13,307,825-13,308,163Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6791003Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr613,307,59313,307,931
    nsv6791003RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr613,307,82513,308,163

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18710326duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18710326Submitted genomicNC_000006.12:g.133
    07593_13307931dup
    GRCh38 (hg38)NC_000006.12Chr613,307,59313,307,931
    nssv18710326RemappedPerfectNC_000006.11:g.133
    07825_13308163dup
    GRCh37.p13First PassNC_000006.11Chr613,307,82513,308,163

    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)
    nssv187103268.1e-0520242946
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