A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586152



Internal ID7057534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31356709..31359968hg38UCSC Ensembl
Innerchr6:31324486..31327745hg19UCSC Ensembl
Innerchr6:31432465..31435724hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg383260
hg193260
hg183260
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998282
Supporting Variants
SamplesHuRef
Known GenesHLA-B
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586152
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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