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nsv6892734

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:308,799

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3273 SVs from 96 studies. See in: genome view    
    Submitted genomic132,836,257-133,145,055Question Mark
    Overlapping variant regions from other studies: 3273 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):134,649,761-134,958,559Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6892734Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10132,836,257133,145,055
    nsv6892734RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10134,649,761134,958,559

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18576733duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18576733Submitted genomicNC_000010.11:g.132
    836257_133145055du
    p
    GRCh38 (hg38)NC_000010.11Chr10132,836,257133,145,055
    nssv18576733RemappedPerfectNC_000010.10:g.134
    649761_134958559du
    p
    GRCh37.p13First PassNC_000010.10Chr10134,649,761134,958,559

    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)
    nssv185767331.1e-053270382
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