A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275382



Internal ID348288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85866705..85866723hg38UCSC Ensembl
Outerchr16:85864270..85867002hg38UCSC Ensembl
Innerchr16:85900311..85900329hg19UCSC Ensembl
Outerchr16:85897876..85900608hg19UCSC Ensembl
Innerchr16:84457812..84457830hg18UCSC Ensembl
Outerchr16:84455377..84458109hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382733
hg192733
hg182733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2586095
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)esv275382
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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