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nsv7082042

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,362

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 301 SVs from 34 studies. See in: genome view    
    Submitted genomic97,527,341-97,544,702Question Mark
    Overlapping variant regions from other studies: 301 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):96,782,340-96,799,701Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7082042Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX97,527,34197,544,702
    nsv7082042RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX96,782,34096,799,701

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18462288deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18462288Submitted genomicNC_000023.11:g.975
    27341_97544702del
    GRCh38 (hg38)NC_000023.11ChrX97,527,34197,544,702
    nssv18462288RemappedPerfectNC_000023.10:g.967
    82340_96799701del
    GRCh37.p13First PassNC_000023.10ChrX96,782,34096,799,701

    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)
    nssv184622885e-061200000
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