A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2275n100



Internal ID22788362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20376297..20422227hg38UCSC Ensembl
chr15:20581550..20627480hg19UCSC Ensembl
chr15:18841564..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3845931
hg1945931
hg1845931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043884, nsv1042994, nsv1044610, nsv1036976, nsv1036122, nsv1039725, nsv1037819, nsv1042618, nsv1047067, nsv1051670
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)dgv2275n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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