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nsv6959102

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:903

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 152 SVs from 26 studies. See in: genome view    
    Submitted genomic2,521,808-2,522,710Question Mark
    Overlapping variant regions from other studies: 152 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):2,571,809-2,572,711Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6959102Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr162,521,8082,522,710
    nsv6959102RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr162,571,8092,572,711

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620893duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620893Submitted genomicNC_000016.10:g.252
    1808_2522710dup
    GRCh38 (hg38)NC_000016.10Chr162,521,8082,522,710
    nssv18620893RemappedPerfectNC_000016.9:g.2571
    809_2572711dup
    GRCh37.p13First PassNC_000016.9Chr162,571,8092,572,711

    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)
    nssv186208934e-061257236
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