A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275435



Internal ID348341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31554183..31554885hg38UCSC Ensembl
Outerchr16:31549357..31556201hg38UCSC Ensembl
Innerchr16:31565504..31566206hg19UCSC Ensembl
Outerchr16:31560678..31567522hg19UCSC Ensembl
Innerchr16:31473005..31473707hg18UCSC Ensembl
Outerchr16:31468179..31475023hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg386845
hg196845
hg186845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585902
Samples
Known Genes
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275435
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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