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nsv7072609

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,843

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 312 SVs from 22 studies. See in: genome view    
    Submitted genomic11,224,588-11,237,430Question Mark
    Overlapping variant regions from other studies: 313 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):11,242,708-11,255,550Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072609Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX11,224,58811,237,430
    nsv7072609RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX11,242,70811,255,550

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18457407deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18457407Submitted genomicNC_000023.11:g.112
    24588_11237430del
    GRCh38 (hg38)NC_000023.11ChrX11,224,58811,237,430
    nssv18457407RemappedPerfectNC_000023.10:g.112
    42708_11255550del
    GRCh37.p13First PassNC_000023.10ChrX11,242,70811,255,550

    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)
    nssv184574076e-0513216667
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