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nsv6928339

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:597

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 300 SVs from 46 studies. See in: genome view    
    Submitted genomic52,321,404-52,322,000Question Mark
    Overlapping variant regions from other studies: 300 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):52,715,188-52,715,784Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6928339Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,321,40452,322,000
    nsv6928339RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1252,715,18852,715,784

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18361995deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18361995Submitted genomicNC_000012.12:g.523
    21404_52322000del
    GRCh38 (hg38)NC_000012.12Chr1252,321,40452,322,000
    nssv18361995RemappedPerfectNC_000012.11:g.527
    15188_52715784del
    GRCh37.p13First PassNC_000012.11Chr1252,715,18852,715,784

    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)
    nssv183619957e-062269546
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