A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274889



Internal ID347849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85150896..85152302hg38UCSC Ensembl
Outerchr16:85150408..85152513hg38UCSC Ensembl
Innerchr16:85184502..85185908hg19UCSC Ensembl
Outerchr16:85184014..85186119hg19UCSC Ensembl
Innerchr16:83742003..83743409hg18UCSC Ensembl
Outerchr16:83741515..83743620hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382106
hg192106
hg182106
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585604, essv2585505
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)esv274889
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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