A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892840



Internal ID19183660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32593089..34034043hg38UCSC Ensembl
Outerchr16:32593089..34068162hg38UCSC Ensembl
Innerchr16:32604410..33836510hg19UCSC Ensembl
Outerchr16:32604410..33870629hg19UCSC Ensembl
Innerchr16:32511911..33744011hg18UCSC Ensembl
Outerchr16:32511911..33778130hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381475074
hg191266220
hg181266220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790490, essv25791746
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892840
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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