A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2274n100



Internal ID22788361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20376297..20411461hg38UCSC Ensembl
chr15:20581550..20616714hg19UCSC Ensembl
chr15:18841564..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3835165
hg1935165
hg1835165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046284, nsv1052970, nsv1052598, nsv1039813, nsv1050822, nsv1053103, nsv1051604
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)dgv2274n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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