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nsv6544104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:526

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 204 SVs from 42 studies. See in: genome view    
    Submitted genomic111,241,681-111,242,206Question Mark
    Overlapping variant regions from other studies: 204 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):111,999,258-111,999,783Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6544104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2111,241,681111,242,206
    nsv6544104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2111,999,258111,999,783

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256489inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256489Submitted genomicNC_000002.12:g.111
    241681_111242206in
    v
    GRCh38 (hg38)NC_000002.12Chr2111,241,681111,242,206
    nssv18256489RemappedPerfectNC_000002.11:g.111
    999258_111999783in
    v
    GRCh37.p13First PassNC_000002.11Chr2111,999,258111,999,783

    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)
    nssv18256489<0.001435260
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