A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104974



Internal ID21270502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135615259..135739997hg38UCSC Ensembl
InnerchrX:134749184..134908428hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38124739
hg19159245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114203
Supporting Variants
Samplessample150
Known GenesCT45A1, CT45A2, CT45A3, CT45A4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104974
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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