nsv6862510

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,725

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 398 SVs from 68 studies. See in: genome view    
    Submitted genomic112,961,471-113,048,195Question Mark
    Overlapping variant regions from other studies: 398 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):115,723,751-115,810,475Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6862510Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9112,961,471113,048,195
    nsv6862510RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,723,751115,810,475

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18560684deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18560684Submitted genomicNC_000009.12:g.112
    961471_113048195de
    l
    GRCh38 (hg38)NC_000009.12Chr9112,961,471113,048,195
    nssv18560684RemappedPerfectNC_000009.11:g.115
    723751_115810475de
    l
    GRCh37.p13First PassNC_000009.11Chr9115,723,751115,810,475

    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)
    nssv185606844e-061268462
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