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nsv7078272

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 266 SVs from 24 studies. See in: genome view    
    Submitted genomic107,188,801-107,191,300Question Mark
    Overlapping variant regions from other studies: 266 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):106,432,031-106,434,530Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7078272Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX107,188,801107,191,300
    nsv7078272RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX106,432,031106,434,530

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18451619deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18451619Submitted genomicNC_000023.11:g.107
    188801_107191300de
    l
    GRCh38 (hg38)NC_000023.11ChrX107,188,801107,191,300
    nssv18451619RemappedPerfectNC_000023.10:g.106
    432031_106434530de
    l
    GRCh37.p13First PassNC_000023.10ChrX106,432,031106,434,530

    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)
    nssv184516199.7e-0521216495
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