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nsv6831892

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 24 studies. See in: genome view    
    Submitted genomic53,693,101-53,695,100Question Mark
    Overlapping variant regions from other studies: 87 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):53,760,794-53,762,793Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6831892Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr753,693,10153,695,100
    nsv6831892RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr753,760,79453,762,793

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18723738duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18723738Submitted genomicNC_000007.14:g.536
    93101_53695100dup
    GRCh38 (hg38)NC_000007.14Chr753,693,10153,695,100
    nssv18723738RemappedPerfectNC_000007.13:g.537
    60794_53762793dup
    GRCh37.p13First PassNC_000007.13Chr753,760,79453,762,793

    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)
    nssv187237384e-061267982
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