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nsv6881675

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 216 SVs from 39 studies. See in: genome view    
    Submitted genomic1,247,001-1,248,000Question Mark
    Overlapping variant regions from other studies: 216 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):1,268,231-1,269,230Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6881675Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr111,247,0011,248,000
    nsv6881675RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr111,268,2311,269,230

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18343956deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18343956Submitted genomicNC_000011.10:g.124
    7001_1248000del
    GRCh38 (hg38)NC_000011.10Chr111,247,0011,248,000
    nssv18343956RemappedPerfectNC_000011.9:g.1268
    231_1269230del
    GRCh37.p13First PassNC_000011.9Chr111,268,2311,269,230

    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)
    nssv183439560.0071841250812
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