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nsv7080971

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:883,582

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1861 SVs from 67 studies. See in: genome view    
    Submitted genomic40,188,484-41,072,065Question Mark
    Overlapping variant regions from other studies: 1862 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):40,047,737-40,931,318Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7080971Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX40,188,48441,072,065
    nsv7080971RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX40,047,73740,931,318

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18656221duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18656221Submitted genomicNC_000023.11:g.401
    88484_41072065dup
    GRCh38 (hg38)NC_000023.11ChrX40,188,48441,072,065
    nssv18656221RemappedPerfectNC_000023.10:g.400
    47737_40931318dup
    GRCh37.p13First PassNC_000023.10ChrX40,047,73740,931,318

    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)
    nssv186562215e-061200000
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