A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788671



Internal ID19170900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55808492..55827882hg38UCSC Ensembl
Innerchr16:55842404..55861794hg19UCSC Ensembl
Innerchr16:54399905..54419295hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3819391
hg1919391
hg1819391
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892862
Supporting Variants
Samples
Known GenesCES1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788671
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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