A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275198



Internal ID348104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52825526..52830795hg38UCSC Ensembl
Outerchr15:52822513..52830808hg38UCSC Ensembl
Innerchr15:53117723..53122992hg19UCSC Ensembl
Outerchr15:53114710..53123005hg19UCSC Ensembl
Innerchr15:50905015..50910284hg18UCSC Ensembl
Outerchr15:50902002..50910297hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg388296
hg198296
hg188296
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585757, essv2586003
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)esv275198
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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