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nsv7030984

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 197 SVs from 38 studies. See in: genome view    
    Submitted genomic63,320,300-63,326,999Question Mark
    Overlapping variant regions from other studies: 197 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):61,951,652-61,958,351Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7030984Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2063,320,30063,326,999
    nsv7030984RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2061,951,65261,958,351

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18435551deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18435551Submitted genomicNC_000020.11:g.633
    20300_63326999del
    GRCh38 (hg38)NC_000020.11Chr2063,320,30063,326,999
    nssv18435551RemappedPerfectNC_000020.10:g.619
    51652_61958351del
    GRCh37.p13First PassNC_000020.10Chr2061,951,65261,958,351

    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)
    nssv184355514e-061276266
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