A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv524n21



Internal ID20132245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114067803..114619628hg38UCSC Ensembl
chrX:113310992..113854086hg19UCSC Ensembl
chrX:113197257..113760342hg18UCSC Ensembl
chrX:113116746..113677066hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38551826
hg19543095
hg18563086
hg17560321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521297, nsv524582
Samples
Known GenesHTR2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv524n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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