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nsv6861205

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 310 SVs from 43 studies. See in: genome view    
    Submitted genomic111,475,501-111,541,400Question Mark
    Overlapping variant regions from other studies: 310 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):114,237,781-114,303,680Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6861205Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9111,475,501111,541,400
    nsv6861205RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9114,237,781114,303,680

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743168duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743168Submitted genomicNC_000009.12:g.111
    475501_111541400du
    p
    GRCh38 (hg38)NC_000009.12Chr9111,475,501111,541,400
    nssv18743168RemappedPerfectNC_000009.11:g.114
    237781_114303680du
    p
    GRCh37.p13First PassNC_000009.11Chr9114,237,781114,303,680

    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)
    nssv18743168<0.00159267228
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