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nsv6710615

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69,667

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 338 SVs from 50 studies. See in: genome view    
    Submitted genomic237,778,462-237,848,128Question Mark
    Overlapping variant regions from other studies: 338 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):238,687,105-238,756,771Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6710615Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2237,778,462237,848,128
    nsv6710615RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2238,687,105238,756,771

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18663773duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18663773Submitted genomicNC_000002.12:g.237
    778462_237848128du
    p
    GRCh38 (hg38)NC_000002.12Chr2237,778,462237,848,128
    nssv18663773RemappedPerfectNC_000002.11:g.238
    687105_238756771du
    p
    GRCh37.p13First PassNC_000002.11Chr2238,687,105238,756,771

    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)
    nssv186637734e-061275482
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