A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2851n100



Internal ID22788938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32069540..32732148hg38UCSC Ensembl
chr16:32080861..32743469hg19UCSC Ensembl
chr16:31988362..32650970hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38662609
hg19662609
hg18662609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065059, nsv1059008, nsv1057368, nsv1057227
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)dgv2851n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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