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nsv6987594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101,892

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 478 SVs from 65 studies. See in: genome view    
    Submitted genomic23,451,879-23,553,770Question Mark
    Overlapping variant regions from other studies: 478 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):23,463,200-23,565,091Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6987594Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1623,451,87923,553,770
    nsv6987594RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1623,463,20023,565,091

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620800duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620800Submitted genomicNC_000016.10:g.234
    51879_23553770dup
    GRCh38 (hg38)NC_000016.10Chr1623,451,87923,553,770
    nssv18620800RemappedPerfectNC_000016.9:g.2346
    3200_23565091dup
    GRCh37.p13First PassNC_000016.9Chr1623,463,20023,565,091

    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)
    nssv186208002.1e-056275126
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