A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586178



Internal ID7057560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28584069..28665552hg38UCSC Ensembl
Innerchr15:28829215..28910698hg19UCSC Ensembl
Innerchr15:26628256..26709739hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3881484
hg1981484
hg1881484
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994657
Supporting Variants
SamplesHuRef
Known GenesHERC2P9
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586178
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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