A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275476



Internal ID1696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38774682..38775147hg38UCSC Ensembl
Outerchr4:38774614..38775185hg38UCSC Ensembl
Innerchr4:38776303..38776768hg19UCSC Ensembl
Outerchr4:38776235..38776806hg19UCSC Ensembl
Innerchr4:38452698..38453163hg18UCSC Ensembl
Outerchr4:38452630..38453201hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38572
hg19572
hg18572
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585822, essv2585611
Samples
Known GenesTLR10
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275476
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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