A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800109



Internal ID18830247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5316436..5404485hg38UCSC Ensembl
Innerchr16:5366437..5454486hg19UCSC Ensembl
Innerchr16:5306438..5394487hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3888050
hg1988050
hg1888050
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892764
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800109
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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