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nsv6977530

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 33 studies. See in: genome view    
    Submitted genomic72,425,701-72,439,700Question Mark
    Overlapping variant regions from other studies: 142 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):72,718,042-72,732,041Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977530Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1572,425,70172,439,700
    nsv6977530RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1572,718,04272,732,041

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18396607deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18396607Submitted genomicNC_000015.10:g.724
    25701_72439700del
    GRCh38 (hg38)NC_000015.10Chr1572,425,70172,439,700
    nssv18396607RemappedPerfectNC_000015.9:g.7271
    8042_72732041del
    GRCh37.p13First PassNC_000015.9Chr1572,718,04272,732,041

    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)
    nssv18396607<0.00156252468
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