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nsv7085074

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:350,708

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 881 SVs from 68 studies. See in: genome view    
    Submitted genomic147,030,159-147,380,866Question Mark
    Overlapping variant regions from other studies: 878 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):146,111,677-146,462,384Question Mark
    Overlapping variant regions from other studies: 311 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):2,554,550-2,905,257Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7085074Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX147,030,159147,380,866
    nsv7085074RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000023.10ChrX146,111,677146,462,384
    nsv7085074RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004070890.2ChrX|NW_00
    4070890.2
    2,554,5502,905,257

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655807duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655807Submitted genomicNC_000023.11:g.147
    030159_147380866du
    p
    GRCh38 (hg38)NC_000023.11ChrX147,030,159147,380,866
    nssv18655807RemappedPerfectNW_004070890.2:g.2
    554550_2905257dup
    GRCh37.p13First PassNW_004070890.2ChrX|NW_00
    4070890.2
    2,554,5502,905,257
    nssv18655807RemappedPerfectNC_000023.10:g.146
    111677_146462384du
    p
    GRCh37.p13Second PassNC_000023.10ChrX146,111,677146,462,384

    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)
    nssv186558075e-061200000
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