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nsv6770994

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60,397

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 203 SVs from 36 studies. See in: genome view    
    Submitted genomic36,215,312-36,275,708Question Mark
    Overlapping variant regions from other studies: 203 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):36,215,414-36,275,810Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6770994Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr536,215,31236,275,708
    nsv6770994RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr536,215,41436,275,810

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18703977duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18703977Submitted genomicNC_000005.10:g.362
    15312_36275708dup
    GRCh38 (hg38)NC_000005.10Chr536,215,31236,275,708
    nssv18703977RemappedPerfectNC_000005.9:g.3621
    5414_36275810dup
    GRCh37.p13First PassNC_000005.9Chr536,215,41436,275,810

    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)
    nssv187039771.4e-054274640
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