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nsv7052928

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,420,431

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4613 SVs from 112 studies. See in: genome view    
    Submitted genomic131,584,338-133,004,768Question Mark
    Overlapping variant regions from other studies: 4742 SVs from 112 studies. See in: genome view    
    Remapped(Score: Perfect):132,341,911-133,762,341Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052928Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,584,338133,004,768
    nsv7052928RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,341,911133,762,341

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767630inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767630Submitted genomicNC_000002.12:g.131
    584338_133004768in
    v
    GRCh38 (hg38)NC_000002.12Chr2131,584,338133,004,768
    nssv18767630RemappedPerfectNC_000002.11:g.132
    341911_133762341in
    v
    GRCh37.p13First PassNC_000002.11Chr2132,341,911133,762,341

    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)
    nssv187676302.9e-058274724
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