U.S. flag

An official website of the United States government

nsv7083371

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,863,376

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7144 SVs from 81 studies. See in: genome view    
    Submitted genomic121,591,286-126,454,661Question Mark
    Overlapping variant regions from other studies: 7152 SVs from 81 studies. See in: genome view    
    Remapped(Score: Good):120,725,140-125,588,644Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7083371Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX121,591,286126,454,661
    nsv7083371RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX120,725,140125,588,644

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18652870duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18652870Submitted genomicNC_000023.11:g.121
    591286_126454661du
    p
    GRCh38 (hg38)NC_000023.11ChrX121,591,286126,454,661
    nssv18652870RemappedGoodNC_000023.10:g.120
    725140_125588644du
    p
    GRCh37.p13First PassNC_000023.10ChrX120,725,140125,588,644

    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)
    nssv18652870<0.00143217172
    Support Center