A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3884n100



Internal ID22789971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:81960795..82093303hg38UCSC Ensembl
chr2:82187919..82320427hg19UCSC Ensembl
chr2:82041430..82173938hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38132509
hg19132509
hg18132509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001699, nsv1001839, nsv1010320, nsv1012707, nsv1011104, nsv998473, nsv999204, nsv1000739, nsv1004404, nsv1005083, nsv1013460
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3884n100
Frequency
Sample Size11257
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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