A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892846



Internal ID19183666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32153014..32363103hg38UCSC Ensembl
Outerchr16:32153014..32363103hg38UCSC Ensembl
Innerchr16:32164335..32374424hg19UCSC Ensembl
Outerchr16:32164335..32374424hg19UCSC Ensembl
Innerchr16:32071836..32281925hg18UCSC Ensembl
Outerchr16:32071836..32281925hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38210090
hg19210090
hg18210090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792927
Samples
Known GenesLOC390705, TP53TG3D
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892846
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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