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nsv7082041

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:225

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 277 SVs from 22 studies. See in: genome view    
    Submitted genomic97,525,683-97,525,907Question Mark
    Overlapping variant regions from other studies: 277 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):96,780,682-96,780,906Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7082041Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX97,525,68397,525,907
    nsv7082041RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX96,780,68296,780,906

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18658714duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18658714Submitted genomicNC_000023.11:g.975
    25683_97525907dup
    GRCh38 (hg38)NC_000023.11ChrX97,525,68397,525,907
    nssv18658714RemappedPerfectNC_000023.10:g.967
    80682_96780906dup
    GRCh37.p13First PassNC_000023.10ChrX96,780,68296,780,906

    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)
    nssv186587145e-061200000
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