U.S. flag

An official website of the United States government

nsv7028199

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,821

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 26 studies. See in: genome view    
    Submitted genomic36,502,101-36,508,921Question Mark
    Overlapping variant regions from other studies: 113 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):36,898,148-36,904,968Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7028199Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2236,502,10136,508,921
    nsv7028199RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2236,898,14836,904,968

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18453802deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18453802Submitted genomicNC_000022.11:g.365
    02101_36508921del
    GRCh38 (hg38)NC_000022.11Chr2236,502,10136,508,921
    nssv18453802RemappedPerfectNC_000022.10:g.368
    98148_36904968del
    GRCh37.p13First PassNC_000022.10Chr2236,898,14836,904,968

    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)
    nssv184538021.5e-054254182
    Support Center