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nsv6915830

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,072

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 39 studies. See in: genome view    
    Submitted genomic2,300,347-2,305,418Question Mark
    Overlapping variant regions from other studies: 169 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):2,321,577-2,326,648Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6915830Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr112,300,3472,305,418
    nsv6915830RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr112,321,5772,326,648

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18345566deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18345566Submitted genomicNC_000011.10:g.230
    0347_2305418del
    GRCh38 (hg38)NC_000011.10Chr112,300,3472,305,418
    nssv18345566RemappedPerfectNC_000011.9:g.2321
    577_2326648del
    GRCh37.p13First PassNC_000011.9Chr112,321,5772,326,648

    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)
    nssv183455664e-061276204
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