A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585591



Internal ID347170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86360257..86361513hg38UCSC Ensembl
Outerchr16:86358843..86362041hg38UCSC Ensembl
Innerchr16:86393863..86395119hg19UCSC Ensembl
Outerchr16:86392449..86395647hg19UCSC Ensembl
Innerchr16:84951364..84952620hg18UCSC Ensembl
Outerchr16:84949950..84953148hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg383199
hg193199
hg183199
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275501
Supporting Variants
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)essv2585591
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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