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nsv6708057

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:602,561

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1520 SVs from 75 studies. See in: genome view    
    Submitted genomic235,965,559-236,568,119Question Mark
    Overlapping variant regions from other studies: 1520 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):236,874,203-237,476,762Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6708057Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2235,965,559236,568,119
    nsv6708057RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2236,874,203237,476,762

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18663580duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18663580Submitted genomicNC_000002.12:g.235
    965559_236568119du
    p
    GRCh38 (hg38)NC_000002.12Chr2235,965,559236,568,119
    nssv18663580RemappedPerfectNC_000002.11:g.236
    874203_237476762du
    p
    GRCh37.p13First PassNC_000002.11Chr2236,874,203237,476,762

    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)
    nssv186635807e-062275322
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