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nsv6532536

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,314

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
    Submitted genomic12,121,083-12,135,396Question Mark
    Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):12,231,898-12,246,211Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6532536Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1912,121,08312,135,396
    nsv6532536RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1912,231,89812,246,211

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18044912deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18044912Submitted genomicNC_000019.10:g.121
    21083_12135396del
    GRCh38 (hg38)NC_000019.10Chr1912,121,08312,135,396
    nssv18044912RemappedPerfectNC_000019.9:g.1223
    1898_12246211del
    GRCh37.p13First PassNC_000019.9Chr1912,231,89812,246,211

    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)
    nssv18044912<0.001139180
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