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nsv6646431

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,057

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
    Submitted genomic19,615,649-19,618,705Question Mark
    Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):19,942,143-19,945,199Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6646431Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,615,64919,618,705
    nsv6646431RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr119,942,14319,945,199

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18365955deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18365955Submitted genomicNC_000001.11:g.196
    15649_19618705del
    GRCh38 (hg38)NC_000001.11Chr119,615,64919,618,705
    nssv18365955RemappedPerfectNC_000001.10:g.199
    42143_19945199del
    GRCh37.p13First PassNC_000001.10Chr119,942,14319,945,199

    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)
    nssv183659553.9e-0511275036
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