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nsv6937489

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 21 studies. See in: genome view    
    Submitted genomic13,826,971-13,826,995Question Mark
    Overlapping variant regions from other studies: 119 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):13,979,905-13,979,929Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6937489Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1213,826,97113,826,995
    nsv6937489RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1213,979,90513,979,929

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18358641deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18358641Submitted genomicNC_000012.12:g.138
    26971_13826995del
    GRCh38 (hg38)NC_000012.12Chr1213,826,97113,826,995
    nssv18358641RemappedPerfectNC_000012.11:g.139
    79905_13979929del
    GRCh37.p13First PassNC_000012.11Chr1213,979,90513,979,929

    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)
    nssv18358641<0.00129251204
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