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nsv6542208

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:969

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 29 studies. See in: genome view    
    Submitted genomic168,176,622-168,177,590Question Mark
    Overlapping variant regions from other studies: 139 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):168,145,860-168,146,828Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6542208Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1168,176,622168,177,590
    nsv6542208RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1168,145,860168,146,828

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18248047inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18248047Submitted genomicNC_000001.11:g.168
    176622_168177590in
    v
    GRCh38 (hg38)NC_000001.11Chr1168,176,622168,177,590
    nssv18248047RemappedPerfectNC_000001.10:g.168
    145860_168146828in
    v
    GRCh37.p13First PassNC_000001.10Chr1168,145,860168,146,828

    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)
    nssv18248047<0.001434054
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