A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586485



Internal ID6711181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:93822871..93825681hg38UCSC Ensembl
Innerchr1:94288427..94291237hg19UCSC Ensembl
Innerchr1:94061015..94063825hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382811
hg192811
hg182811
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988321
Supporting Variants
SamplesHuRef
Known GenesBCAR3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586485
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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