A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4526n54



Internal ID20137950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50582767..51475068hg38UCSC Ensembl
chr15:50874964..51767265hg19UCSC Ensembl
chr15:48662256..49554557hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38892302
hg19892302
hg18892302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569399, nsv569400
Samples
Known GenesAP4E1, CYP19A1, DCAF13P3, DMXL2, GLDN, MIR4713, SPPL2A, TNFAIP8L3, TRPM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4526n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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