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nsv7083706

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:161,162

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 512 SVs from 57 studies. See in: genome view    
    Submitted genomic130,425,150-130,586,311Question Mark
    Overlapping variant regions from other studies: 512 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):129,559,124-129,720,285Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7083706Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX130,425,150130,586,311
    nsv7083706RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX129,559,124129,720,285

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18458516deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18458516Submitted genomicNC_000023.11:g.130
    425150_130586311de
    l
    GRCh38 (hg38)NC_000023.11ChrX130,425,150130,586,311
    nssv18458516RemappedPerfectNC_000023.10:g.129
    559124_129720285de
    l
    GRCh37.p13First PassNC_000023.10ChrX129,559,124129,720,285

    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)
    nssv184585165e-061200000
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