A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788037



Internal ID19170012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2649303..2693417hg38UCSC Ensembl
Innerchr16:2699304..2743418hg19UCSC Ensembl
Innerchr16:2639305..2683419hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3844115
hg1944115
hg1844115
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892757
Supporting Variants
Samples
Known GenesERVK13-1, KCTD5
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788037
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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