A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2225n100



Internal ID22788312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20267586..20418941hg38UCSC Ensembl
chr15:20472839..20624194hg19UCSC Ensembl
chr15:18732853..18884208hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38151356
hg19151356
hg18151356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038193, nsv1038207, nsv1052906, nsv1045419, nsv1036362
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2225n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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