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nsv6532183

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 25 studies. See in: genome view    
    Submitted genomic51,577,830-51,591,929Question Mark
    Overlapping variant regions from other studies: 96 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):52,081,083-52,095,182Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6532183Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1951,577,83051,591,929
    nsv6532183RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1952,081,08352,095,182

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18048724deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18048724Submitted genomicNC_000019.10:g.515
    77830_51591929del
    GRCh38 (hg38)NC_000019.10Chr1951,577,83051,591,929
    nssv18048724RemappedPerfectNC_000019.9:g.5208
    1083_52095182del
    GRCh37.p13First PassNC_000019.9Chr1952,081,08352,095,182

    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)
    nssv18048724<0.001139256
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