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nsv7090651

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 314 SVs from 24 studies. See in: genome view    
    Submitted genomic103,788,901-103,802,000Question Mark
    Overlapping variant regions from other studies: 314 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):103,043,830-103,056,929Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7090651Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX103,788,901103,802,000
    nsv7090651RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX103,043,830103,056,929

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18457210deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18457210Submitted genomicNC_000023.11:g.103
    788901_103802000de
    l
    GRCh38 (hg38)NC_000023.11ChrX103,788,901103,802,000
    nssv18457210RemappedPerfectNC_000023.10:g.103
    043830_103056929de
    l
    GRCh37.p13First PassNC_000023.10ChrX103,043,830103,056,929

    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)
    nssv18457210<0.00142216495
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