A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798910



Internal ID18825921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82684425..82732002hg38UCSC Ensembl
Innerchr16:82718030..82765607hg19UCSC Ensembl
Innerchr16:81275531..81323108hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3847578
hg1947578
hg1847578
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892916
Supporting Variants
Samples
Known GenesCDH13, MIR8058
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798910
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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