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nsv7044993

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,683,161

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10190 SVs from 87 studies. See in: genome view    
    Submitted genomic104,618,913-113,302,073Question Mark
    Overlapping variant regions from other studies: 10172 SVs from 87 studies. See in: genome view    
    Remapped(Score: Good):103,863,594-112,545,300Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044993Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX104,618,913113,302,073
    nsv7044993RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX103,863,594112,545,300

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765597inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765597Submitted genomicNC_000023.11:g.104
    618913_113302073in
    v
    GRCh38 (hg38)NC_000023.11ChrX104,618,913113,302,073
    nssv18765597RemappedGoodNC_000023.10:g.103
    863594_112545300in
    v
    GRCh37.p13First PassNC_000023.10ChrX103,863,594112,545,300

    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)
    nssv187655975e-061200000
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