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nsv6913930

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,156,087

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2367 SVs from 93 studies. See in: genome view    
    Submitted genomic11,423,524-12,579,610Question Mark
    Overlapping variant regions from other studies: 2367 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):11,445,071-12,601,157Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6913930Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1111,423,52412,579,610
    nsv6913930RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1111,445,07112,601,157

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18343058deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18343058Submitted genomicNC_000011.10:g.114
    23524_12579610del
    GRCh38 (hg38)NC_000011.10Chr1111,423,52412,579,610
    nssv18343058RemappedPerfectNC_000011.9:g.1144
    5071_12601157del
    GRCh37.p13First PassNC_000011.9Chr1111,445,07112,601,157

    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)
    nssv183430584e-061275804
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