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nsv6931418

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,449

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 461 SVs from 68 studies. See in: genome view    
    Submitted genomic8,208,854-8,238,302Question Mark
    Overlapping variant regions from other studies: 461 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):8,361,450-8,390,898Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6931418Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr128,208,8548,238,302
    nsv6931418RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr128,361,4508,390,898

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18599472duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18599472Submitted genomicNC_000012.12:g.820
    8854_8238302dup
    GRCh38 (hg38)NC_000012.12Chr128,208,8548,238,302
    nssv18599472RemappedPerfectNC_000012.11:g.836
    1450_8390898dup
    GRCh37.p13First PassNC_000012.11Chr128,361,4508,390,898

    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)
    nssv185994720.1437677264850
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