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nsv7082046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:410

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 278 SVs from 23 studies. See in: genome view    
    Submitted genomic97,558,639-97,559,048Question Mark
    Overlapping variant regions from other studies: 278 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):96,813,638-96,814,047Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7082046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX97,558,63997,559,048
    nsv7082046RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX96,813,63896,814,047

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18462290deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18462290Submitted genomicNC_000023.11:g.975
    58639_97559048del
    GRCh38 (hg38)NC_000023.11ChrX97,558,63997,559,048
    nssv18462290RemappedPerfectNC_000023.10:g.968
    13638_96814047del
    GRCh37.p13First PassNC_000023.10ChrX96,813,63896,814,047

    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)
    nssv184622907.4e-0516216216
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