A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2264n100



Internal ID22788351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20364686..20411461hg38UCSC Ensembl
chr15:20569939..20616714hg19UCSC Ensembl
chr15:18829953..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3846776
hg1946776
hg1846776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040927, nsv1049018, nsv1040677, nsv1039450
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2264n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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