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nsv7085079

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 279 SVs from 18 studies. See in: genome view    
    Submitted genomic14,706,062-14,706,110Question Mark
    Overlapping variant regions from other studies: 280 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):14,724,184-14,724,232Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7085079Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX14,706,06214,706,110
    nsv7085079RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX14,724,18414,724,232

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18458954deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18458954Submitted genomicNC_000023.11:g.147
    06062_14706110del
    GRCh38 (hg38)NC_000023.11ChrX14,706,06214,706,110
    nssv18458954RemappedPerfectNC_000023.10:g.147
    24184_14724232del
    GRCh37.p13First PassNC_000023.10ChrX14,724,18414,724,232

    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)
    nssv184589540.44195544216676
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