A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790587



Internal ID19180367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32128300..32586373hg38UCSC Ensembl
Innerchr16:32139621..32597694hg19UCSC Ensembl
Innerchr16:32047122..32505195hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38458074
hg19458074
hg18458074
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892833
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=159
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790587
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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