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nsv6930281

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 18 studies. See in: genome view    
    Submitted genomic27,619,239-27,619,279Question Mark
    Overlapping variant regions from other studies: 83 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):28,193,376-28,193,416Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930281Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1327,619,23927,619,279
    nsv6930281RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1328,193,37628,193,416

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18376764deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18376764Submitted genomicNC_000013.11:g.276
    19239_27619279del
    GRCh38 (hg38)NC_000013.11Chr1327,619,23927,619,279
    nssv18376764RemappedPerfectNC_000013.10:g.281
    93376_28193416del
    GRCh37.p13First PassNC_000013.10Chr1328,193,37628,193,416

    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)
    nssv183767640.06114724241866
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