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nsv7086375

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:743,010

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1103 SVs from 61 studies. See in: genome view    
    Submitted genomic25,891,683-26,634,692Question Mark
    Overlapping variant regions from other studies: 1104 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):25,909,800-26,652,809Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7086375Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX25,891,68326,634,692
    nsv7086375RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX25,909,80026,652,809

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18655270duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18655270Submitted genomicNC_000023.11:g.258
    91683_26634692dup
    GRCh38 (hg38)NC_000023.11ChrX25,891,68326,634,692
    nssv18655270RemappedPerfectNC_000023.10:g.259
    09800_26652809dup
    GRCh37.p13First PassNC_000023.10ChrX25,909,80026,652,809

    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)
    nssv186552705e-061200000
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