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nsv6546015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:521

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 185 SVs from 28 studies. See in: genome view    
    Submitted genomic169,489,421-169,489,941Question Mark
    Overlapping variant regions from other studies: 185 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):170,345,931-170,346,451Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6546015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2169,489,421169,489,941
    nsv6546015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2170,345,931170,346,451

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256285inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256285Submitted genomicNC_000002.12:g.169
    489421_169489941in
    v
    GRCh38 (hg38)NC_000002.12Chr2169,489,421169,489,941
    nssv18256285RemappedPerfectNC_000002.11:g.170
    345931_170346451in
    v
    GRCh37.p13First PassNC_000002.11Chr2170,345,931170,346,451

    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)
    nssv18256285<0.001137172
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