A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv526n21



Internal ID22766718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116458613..116619653hg38UCSC Ensembl
chrX:115589779..115753621hg19UCSC Ensembl
chrX:115503807..115637649hg18UCSC Ensembl
chrX:115401661..115535503hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38161041
hg19163843
hg18133843
hg17133843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv524543, nsv526134
Samples
Known GenesCXorf61, SLC6A14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv526n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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