A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587102



Internal ID7058484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2042513..2070610hg38UCSC Ensembl
Innerchr11:2063743..2091840hg19UCSC Ensembl
Innerchr11:2020319..2048416hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3828098
hg1928098
hg1828098
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992756
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587102
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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