A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275567



Internal ID1787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:91889277..91889326hg38UCSC Ensembl
Outerchr15:91888695..91889482hg38UCSC Ensembl
Innerchr15:92432507..92432556hg19UCSC Ensembl
Outerchr15:92431925..92432712hg19UCSC Ensembl
Innerchr15:90233511..90233560hg18UCSC Ensembl
Outerchr15:90232929..90233716hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38788
hg19788
hg18788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2586013
Samples
Known GenesSLCO3A1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275567
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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