A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3886n100



Internal ID20155502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86721712..86945592hg38UCSC Ensembl
chr2:86948835..87172715hg19UCSC Ensembl
chr2:86802346..87026226hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38223881
hg19223881
hg18223881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008817, nsv1007746, nsv1002420
Samples
Known GenesANAPC1P1, CD8A, CD8B, RGPD1, RGPD2, RMND5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3886n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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