A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782385



Internal ID18830951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21569823..21726454hg38UCSC Ensembl
Innerchr16:21581144..21737775hg19UCSC Ensembl
Innerchr16:21488645..21645276hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38156632
hg19156632
hg18156632
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892812
Supporting Variants
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782385
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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