A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587178



Internal ID6711874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:41277708..41278892hg38UCSC Ensembl
Innerchr20:39906348..39907532hg19UCSC Ensembl
Innerchr20:39339762..39340946hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381185
hg191185
hg181185
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990825
Supporting Variants
SamplesHuRef
Known GenesZHX3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587178
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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