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nsv7076275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,147

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 610 SVs from 39 studies. See in: genome view    
    Submitted genomic6,943,518-6,958,664Question Mark
    Overlapping variant regions from other studies: 611 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):6,861,559-6,876,705Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX6,943,5186,958,664
    nsv7076275RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX6,861,5596,876,705

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18461408deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18461408Submitted genomicNC_000023.11:g.694
    3518_6958664del
    GRCh38 (hg38)NC_000023.11ChrX6,943,5186,958,664
    nssv18461408RemappedPerfectNC_000023.10:g.686
    1559_6876705del
    GRCh37.p13First PassNC_000023.10ChrX6,861,5596,876,705

    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)
    nssv184614085e-061200000
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