A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2491n100



Internal ID22788578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28176880..28713634hg38UCSC Ensembl
chr15:28422026..28958780hg19UCSC Ensembl
chr15:26095621..26757821hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38536755
hg19536755
hg18662201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052642, nsv1044648
Samples
Known GenesGOLGA8F, GOLGA8G, GOLGA8M, HERC2, 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)dgv2491n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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