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nsv6904226

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60,572

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 216 SVs from 42 studies. See in: genome view    
    Submitted genomic56,762,134-56,822,705Question Mark
    Overlapping variant regions from other studies: 218 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):56,529,610-56,590,181Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6904226Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1156,762,13456,822,705
    nsv6904226RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1156,529,61056,590,181

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18576736duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18576736Submitted genomicNC_000011.10:g.567
    62134_56822705dup
    GRCh38 (hg38)NC_000011.10Chr1156,762,13456,822,705
    nssv18576736RemappedPerfectNC_000011.9:g.5652
    9610_56590181dup
    GRCh37.p13First PassNC_000011.9Chr1156,529,61056,590,181

    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)
    nssv185767364e-061274656
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