A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2852n100



Internal ID22788939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32102349..32732148hg38UCSC Ensembl
chr16:32113670..32743469hg19UCSC Ensembl
chr16:32021171..32650970hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38629800
hg19629800
hg18629800
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066586, nsv1055488, nsv1055610, nsv1066536, nsv1064065
Samples
Known GenesHERC2P4, LOC390705, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2852n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss8
Observed Complex0
Frequencyn/a


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