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nsv6542672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:168

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 19 studies. See in: genome view    
    Submitted genomic196,886,972-196,887,139Question Mark
    Overlapping variant regions from other studies: 151 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):197,751,696-197,751,863Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6542672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2196,886,972196,887,139
    nsv6542672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2197,751,696197,751,863

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18257072inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18257072Submitted genomicNC_000002.12:g.196
    886972_196887139in
    v
    GRCh38 (hg38)NC_000002.12Chr2196,886,972196,887,139
    nssv18257072RemappedPerfectNC_000002.11:g.197
    751696_197751863in
    v
    GRCh37.p13First PassNC_000002.11Chr2197,751,696197,751,863

    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)
    nssv18257072<0.001136408
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