A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798082



Internal ID18826012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89353948..89396270hg38UCSC Ensembl
Innerchr16:89420356..89462678hg19UCSC Ensembl
Innerchr16:87947857..87990179hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3842323
hg1942323
hg1842323
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892940
Supporting Variants
Samples
Known GenesANKRD11
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798082
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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