A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586137



Internal ID6710833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1028440..1029100hg38UCSC Ensembl
Innerchr1:963820..964480hg19UCSC Ensembl
Innerchr1:953683..954343hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38661
hg19661
hg18661
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv987912
Supporting Variants
SamplesHuRef
Known GenesAGRN
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586137
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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