A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788239



Internal ID19173642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5897601..5968603hg38UCSC Ensembl
Innerchr16:5947602..6018604hg19UCSC Ensembl
Innerchr16:5887603..5958605hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3871003
hg1971003
hg1871003
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892766
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=34
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788239
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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