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nsv7059174

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 377 SVs from 27 studies. See in: genome view    
    Submitted genomic4,617,801-4,633,900Question Mark
    Overlapping variant regions from other studies: 378 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):4,535,842-4,551,941Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059174Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX4,617,8014,633,900
    nsv7059174RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX4,535,8424,551,941

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18656888duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18656888Submitted genomicNC_000023.11:g.461
    7801_4633900dup
    GRCh38 (hg38)NC_000023.11ChrX4,617,8014,633,900
    nssv18656888RemappedPerfectNC_000023.10:g.453
    5842_4551941dup
    GRCh37.p13First PassNC_000023.10ChrX4,535,8424,551,941

    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)
    nssv186568885e-061200000
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