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nsv7078270

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:210,936

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 469 SVs from 47 studies. See in: genome view    
    Submitted genomic107,187,351-107,398,286Question Mark
    Overlapping variant regions from other studies: 469 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):106,430,581-106,641,516Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7078270Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX107,187,351107,398,286
    nsv7078270RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX106,430,581106,641,516

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18653439duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18653439Submitted genomicNC_000023.11:g.107
    187351_107398286du
    p
    GRCh38 (hg38)NC_000023.11ChrX107,187,351107,398,286
    nssv18653439RemappedPerfectNC_000023.10:g.106
    430581_106641516du
    p
    GRCh37.p13First PassNC_000023.10ChrX106,430,581106,641,516

    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)
    nssv186534399e-062222222
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