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nsv6544748

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:682

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 221 SVs from 30 studies. See in: genome view    
    Submitted genomic43,772,365-43,773,046Question Mark
    Overlapping variant regions from other studies: 221 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):45,192,246-45,192,927Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6544748Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2143,772,36543,773,046
    nsv6544748RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2145,192,24645,192,927

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18204116duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18204116Submitted genomicNC_000021.9:g.4377
    2365_43773046dup
    GRCh38 (hg38)NC_000021.9Chr2143,772,36543,773,046
    nssv18204116RemappedPerfectNC_000021.8:g.4519
    2246_45192927dup
    GRCh37.p13First PassNC_000021.8Chr2145,192,24645,192,927

    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)
    nssv18204116<0.001338540
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