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nsv6915481

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:904,830

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2475 SVs from 97 studies. See in: genome view    
    Submitted genomic7,014,782-7,919,611Question Mark
    Overlapping variant regions from other studies: 2504 SVs from 99 studies. See in: genome view    
    Remapped(Score: Good):7,036,013-7,941,158Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6915481Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr117,014,7827,919,611
    nsv6915481RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr117,036,0137,941,158

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18582130duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18582130Submitted genomicNC_000011.10:g.701
    4782_7919611dup
    GRCh38 (hg38)NC_000011.10Chr117,014,7827,919,611
    nssv18582130RemappedGoodNC_000011.9:g.7036
    013_7941158dup
    GRCh37.p13First PassNC_000011.9Chr117,036,0137,941,158

    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)
    nssv185821304e-061274070
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