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nsv7032412

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,389

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 225 SVs from 37 studies. See in: genome view    
    Submitted genomic37,858,110-37,883,498Question Mark
    Overlapping variant regions from other studies: 226 SVs from 37 studies. See in: genome view    
    Remapped(Score: Good):39,230,412-39,255,801Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7032412Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2137,858,11037,883,498
    nsv7032412RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2139,230,41239,255,801

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18437662deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18437662Submitted genomicNC_000021.9:g.3785
    8110_37883498del
    GRCh38 (hg38)NC_000021.9Chr2137,858,11037,883,498
    nssv18437662RemappedGoodNC_000021.8:g.3923
    0412_39255801del
    GRCh37.p13First PassNC_000021.8Chr2139,230,41239,255,801

    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)
    nssv184376624e-061276232
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