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nsv6646899

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:660,857

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1555 SVs from 75 studies. See in: genome view    
    Submitted genomic19,751,232-20,412,088Question Mark
    Overlapping variant regions from other studies: 1555 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):20,077,725-20,738,581Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6646899Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,751,23220,412,088
    nsv6646899RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr120,077,72520,738,581

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18366214deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18366214Submitted genomicNC_000001.11:g.197
    51232_20412088del
    GRCh38 (hg38)NC_000001.11Chr119,751,23220,412,088
    nssv18366214RemappedPerfectNC_000001.10:g.200
    77725_20738581del
    GRCh37.p13First PassNC_000001.10Chr120,077,72520,738,581

    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)
    nssv183662144e-061276224
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