A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797439



Internal ID18821659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84354197..84448953hg38UCSC Ensembl
Innerchr16:84387803..84482559hg19UCSC Ensembl
Innerchr16:82945304..83040060hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3894757
hg1994757
hg1894757
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892928
Supporting Variants
Samples
Known GenesATP2C2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=68
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797439
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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