A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275183



Internal ID348089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34856504..34858698hg38UCSC Ensembl
Outerchr11:34856214..34859829hg38UCSC Ensembl
Innerchr11:34878051..34880245hg19UCSC Ensembl
Outerchr11:34877761..34881376hg19UCSC Ensembl
Innerchr11:34834627..34836821hg18UCSC Ensembl
Outerchr11:34834337..34837952hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383616
hg193616
hg183616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585537
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)esv275183
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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