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nsv6966951

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,266,901

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2950 SVs from 87 studies. See in: genome view    
    Submitted genomic70,353,016-71,619,916Question Mark
    Overlapping variant regions from other studies: 2950 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):70,819,733-72,086,633Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6966951Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1470,353,01671,619,916
    nsv6966951RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1470,819,73372,086,633

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18612732duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18612732Submitted genomicNC_000014.9:g.7035
    3016_71619916dup
    GRCh38 (hg38)NC_000014.9Chr1470,353,01671,619,916
    nssv18612732RemappedPerfectNC_000014.8:g.7081
    9733_72086633dup
    GRCh37.p13First PassNC_000014.8Chr1470,819,73372,086,633

    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)
    nssv186127324e-061275398
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