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nsv6901314

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:202,159

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 507 SVs from 54 studies. See in: genome view    
    Submitted genomic43,487,245-43,689,403Question Mark
    Overlapping variant regions from other studies: 507 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):43,508,795-43,710,953Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6901314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1143,487,24543,689,403
    nsv6901314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1143,508,79543,710,953

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18345783deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18345783Submitted genomicNC_000011.10:g.434
    87245_43689403del
    GRCh38 (hg38)NC_000011.10Chr1143,487,24543,689,403
    nssv18345783RemappedPerfectNC_000011.9:g.4350
    8795_43710953del
    GRCh37.p13First PassNC_000011.9Chr1143,508,79543,710,953

    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)
    nssv183457834e-061276252
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