A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790913



Internal ID19161968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32092598..32491547hg38UCSC Ensembl
Innerchr16:32103919..32502868hg19UCSC Ensembl
Innerchr16:32011420..32410369hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38398950
hg19398950
hg18398950
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=163
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790913
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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