A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585363



Internal ID346942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86719450..86719464hg38UCSC Ensembl
Outerchr16:86719357..86720416hg38UCSC Ensembl
Innerchr16:86753056..86753070hg19UCSC Ensembl
Outerchr16:86752963..86754022hg19UCSC Ensembl
Innerchr16:85310557..85310571hg18UCSC Ensembl
Outerchr16:85310464..85311523hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381060
hg191060
hg181060
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275397
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)essv2585363
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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