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nsv7083638

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:188,379

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 593 SVs from 49 studies. See in: genome view    
    Submitted genomic123,995,175-124,183,553Question Mark
    Overlapping variant regions from other studies: 593 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):123,129,025-123,317,403Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7083638Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX123,995,175124,183,553
    nsv7083638RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX123,129,025123,317,403

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655372duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655372Submitted genomicNC_000023.11:g.123
    995175_124183553du
    p
    GRCh38 (hg38)NC_000023.11ChrX123,995,175124,183,553
    nssv18655372RemappedPerfectNC_000023.10:g.123
    129025_123317403du
    p
    GRCh37.p13First PassNC_000023.10ChrX123,129,025123,317,403

    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)
    nssv186553725e-061200000
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