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nsv7088572

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:259,108

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 612 SVs from 61 studies. See in: genome view    
    Submitted genomic70,051,045-70,310,152Question Mark
    Overlapping variant regions from other studies: 612 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):69,270,895-69,530,002Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7088572Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX70,051,04570,310,152
    nsv7088572RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX69,270,89569,530,002

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659711duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659711Submitted genomicNC_000023.11:g.700
    51045_70310152dup
    GRCh38 (hg38)NC_000023.11ChrX70,051,04570,310,152
    nssv18659711RemappedPerfectNC_000023.10:g.692
    70895_69530002dup
    GRCh37.p13First PassNC_000023.10ChrX69,270,89569,530,002

    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)
    nssv186597115e-061200000
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