A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586904



Internal ID6711600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42628776..42630987hg38UCSC Ensembl
Innerchr5:42628878..42631089hg19UCSC Ensembl
Innerchr5:42664635..42666846hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg382212
hg192212
hg182212
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv996134
Supporting Variants
SamplesHuRef
Known GenesGHR
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586904
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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