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nsv6720530

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:171,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1131 SVs from 77 studies. See in: genome view    
    Submitted genomic39,929,701-40,101,500Question Mark
    Overlapping variant regions from other studies: 1131 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):39,931,321-40,103,120Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6720530Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr439,929,70140,101,500
    nsv6720530RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr439,931,32140,103,120

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18688167duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18688167Submitted genomicNC_000004.12:g.399
    29701_40101500dup
    GRCh38 (hg38)NC_000004.12Chr439,929,70140,101,500
    nssv18688167RemappedPerfectNC_000004.11:g.399
    31321_40103120dup
    GRCh37.p13First PassNC_000004.11Chr439,931,32140,103,120

    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)
    nssv186881678.3e-0522259060
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