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nsv6764929

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 28 studies. See in: genome view    
    Submitted genomic36,244,701-36,248,200Question Mark
    Overlapping variant regions from other studies: 95 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):36,244,803-36,248,302Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6764929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr536,244,70136,248,200
    nsv6764929RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr536,244,80336,248,302

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18703980duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18703980Submitted genomicNC_000005.10:g.362
    44701_36248200dup
    GRCh38 (hg38)NC_000005.10Chr536,244,70136,248,200
    nssv18703980RemappedPerfectNC_000005.9:g.3624
    4803_36248302dup
    GRCh37.p13First PassNC_000005.9Chr536,244,80336,248,302

    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)
    nssv187039805.4e-0515272086
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