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nsv6936132

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,126

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 32 studies. See in: genome view    
    Submitted genomic29,157,732-29,166,857Question Mark
    Overlapping variant regions from other studies: 142 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):29,310,665-29,319,790Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6936132Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1229,157,73229,166,857
    nsv6936132RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1229,310,66529,319,790

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18360812deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18360812Submitted genomicNC_000012.12:g.291
    57732_29166857del
    GRCh38 (hg38)NC_000012.12Chr1229,157,73229,166,857
    nssv18360812RemappedPerfectNC_000012.11:g.293
    10665_29319790del
    GRCh37.p13First PassNC_000012.11Chr1229,310,66529,319,790

    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)
    nssv183608127e-062276222
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