A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792711



Internal ID19172602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27042840..27075347hg38UCSC Ensembl
Innerchr16:27054161..27086668hg19UCSC Ensembl
Innerchr16:26961662..26994169hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3832508
hg1932508
hg1832508
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892820
Supporting Variants
Samples
Known GenesC16orf82
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792711
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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