A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791204



Internal ID19160452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32126644..32611229hg38UCSC Ensembl
Innerchr16:32137965..32622550hg19UCSC Ensembl
Innerchr16:32045466..32530051hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38484586
hg19484586
hg18484586
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=162
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791204
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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