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nsv6713801

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:869,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2850 SVs from 87 studies. See in: genome view    
    Submitted genomic238,741,801-239,611,700Question Mark
    Overlapping variant regions from other studies: 2798 SVs from 87 studies. See in: genome view    
    Remapped(Score: Good):239,650,442-240,533,394Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6713801Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2238,741,801239,611,700
    nsv6713801RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2239,650,442240,533,394

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18663848duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18663848Submitted genomicNC_000002.12:g.238
    741801_239611700du
    p
    GRCh38 (hg38)NC_000002.12Chr2238,741,801239,611,700
    nssv18663848RemappedGoodNC_000002.11:g.239
    650442_240533394du
    p
    GRCh37.p13First PassNC_000002.11Chr2239,650,442240,533,394

    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)
    nssv186638485.7e-0516274336
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