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nsv6976069

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 378 SVs from 43 studies. See in: genome view    
    Submitted genomic80,624,801-80,751,800Question Mark
    Overlapping variant regions from other studies: 378 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):80,917,142-81,044,141Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6976069Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1580,624,80180,751,800
    nsv6976069RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1580,917,14281,044,141

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18621998duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18621998Submitted genomicNC_000015.10:g.806
    24801_80751800dup
    GRCh38 (hg38)NC_000015.10Chr1580,624,80180,751,800
    nssv18621998RemappedPerfectNC_000015.9:g.8091
    7142_81044141dup
    GRCh37.p13First PassNC_000015.9Chr1580,917,14281,044,141

    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)
    nssv186219984e-061275770
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