A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2492n100



Internal ID22788579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28465092..28724519hg38UCSC Ensembl
chr15:28710238..28969665hg19UCSC Ensembl
chr15:26496042..26768706hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38259428
hg19259428
hg18272665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048161, nsv1042040
Samples
Known GenesGOLGA8F, GOLGA8G, GOLGA8M, HERC2P9, MIR4509-1, MIR4509-2, MIR4509-3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2492n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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