A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275494



Internal ID348400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87637813..87639606hg38UCSC Ensembl
Outerchr15:87634151..87640047hg38UCSC Ensembl
Innerchr15:88181044..88182837hg19UCSC Ensembl
Outerchr15:88177382..88183278hg19UCSC Ensembl
Innerchr15:85982048..85983841hg18UCSC Ensembl
Outerchr15:85978386..85984282hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg385897
hg195897
hg185897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585641
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)esv275494
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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