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nsv6793920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:159,872

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 728 SVs from 64 studies. See in: genome view    
    Submitted genomic126,502,747-126,662,618Question Mark
    Overlapping variant regions from other studies: 728 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):125,838,439-125,998,310Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5126,502,747126,662,618
    nsv6793920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5125,838,439125,998,310

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18694677duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18694677Submitted genomicNC_000005.10:g.126
    502747_126662618du
    p
    GRCh38 (hg38)NC_000005.10Chr5126,502,747126,662,618
    nssv18694677RemappedPerfectNC_000005.9:g.1258
    38439_125998310dup
    GRCh37.p13First PassNC_000005.9Chr5125,838,439125,998,310

    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)
    nssv186946771.1e-053275778
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