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nsv6910993

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,570

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 23 studies. See in: genome view    
    Submitted genomic117,199,432-117,203,001Question Mark
    Overlapping variant regions from other studies: 111 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):117,070,148-117,073,717Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6910993Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11117,199,432117,203,001
    nsv6910993RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11117,070,148117,073,717

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18343356deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18343356Submitted genomicNC_000011.10:g.117
    199432_117203001de
    l
    GRCh38 (hg38)NC_000011.10Chr11117,199,432117,203,001
    nssv18343356RemappedPerfectNC_000011.9:g.1170
    70148_117073717del
    GRCh37.p13First PassNC_000011.9Chr11117,070,148117,073,717

    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)
    nssv183433563.2e-059276118
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