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nsv7080920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 374 SVs from 51 studies. See in: genome view    
    Submitted genomic39,720,601-39,795,700Question Mark
    Overlapping variant regions from other studies: 374 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):39,579,855-39,654,954Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7080920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX39,720,60139,795,700
    nsv7080920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX39,579,85539,654,954

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18460552deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18460552Submitted genomicNC_000023.11:g.397
    20601_39795700del
    GRCh38 (hg38)NC_000023.11ChrX39,720,60139,795,700
    nssv18460552RemappedPerfectNC_000023.10:g.395
    79855_39654954del
    GRCh37.p13First PassNC_000023.10ChrX39,579,85539,654,954

    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)
    nssv184605525e-061200000
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