U.S. flag

An official website of the United States government

nsv7067713

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,257

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 494 SVs from 52 studies. See in: genome view    
    Submitted genomic3,680,302-3,711,558Question Mark
    Overlapping variant regions from other studies: 495 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):3,598,343-3,629,599Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067713Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX3,680,3023,711,558
    nsv7067713RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX3,598,3433,629,599

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18455597deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18455597Submitted genomicNC_000023.11:g.368
    0302_3711558del
    GRCh38 (hg38)NC_000023.11ChrX3,680,3023,711,558
    nssv18455597RemappedPerfectNC_000023.10:g.359
    8343_3629599del
    GRCh37.p13First PassNC_000023.10ChrX3,598,3433,629,599

    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)
    nssv184555975e-061200000
    Support Center