A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2395n100



Internal ID22788482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22092910..22215910hg38UCSC Ensembl
chr15:22380861..22503861hg19UCSC Ensembl
chr15:19882225..20005225hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38123001
hg19123001
hg18123001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047793, nsv1040015, nsv1040860
Samples
Known GenesOR4N3P, OR4N4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2395n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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