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nsv6872575

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 281 SVs from 56 studies. See in: genome view    
    Submitted genomic106,979,501-107,043,500Question Mark
    Overlapping variant regions from other studies: 281 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):109,741,782-109,805,781Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6872575Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9106,979,501107,043,500
    nsv6872575RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9109,741,782109,805,781

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18561580deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18561580Submitted genomicNC_000009.12:g.106
    979501_107043500de
    l
    GRCh38 (hg38)NC_000009.12Chr9106,979,501107,043,500
    nssv18561580RemappedPerfectNC_000009.11:g.109
    741782_109805781de
    l
    GRCh37.p13First PassNC_000009.11Chr9109,741,782109,805,781

    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)
    nssv18561580<0.00164250198
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