nsv6806972

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:459,345

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2305 SVs from 88 studies. See in: genome view    
    Submitted genomic1,781,533-2,240,877Question Mark
    Overlapping variant regions from other studies: 2305 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):1,821,169-2,280,512Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6806972Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr71,781,5332,240,877
    nsv6806972RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr71,821,1692,280,512

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18724223duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18724223Submitted genomicNC_000007.14:g.178
    1533_2240877dup
    GRCh38 (hg38)NC_000007.14Chr71,781,5332,240,877
    nssv18724223RemappedPerfectNC_000007.13:g.182
    1169_2280512dup
    GRCh37.p13First PassNC_000007.13Chr71,821,1692,280,512

    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)
    nssv187242234e-061273728
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