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nsv6546843

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:265

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 189 SVs from 38 studies. See in: genome view    
    Submitted genomic108,453,734-108,453,998Question Mark
    Overlapping variant regions from other studies: 189 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):109,070,190-109,070,454Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6546843Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2108,453,734108,453,998
    nsv6546843RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2109,070,190109,070,454

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256450inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256450Submitted genomicNC_000002.12:g.108
    453734_108453998in
    v
    GRCh38 (hg38)NC_000002.12Chr2108,453,734108,453,998
    nssv18256450RemappedPerfectNC_000002.11:g.109
    070190_109070454in
    v
    GRCh37.p13First PassNC_000002.11Chr2109,070,190109,070,454

    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)
    nssv18256450<0.001136746
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