A curated catalogue of human genomic structural variation




Variant Details

Variant: esv987912



Internal ID6723886
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586137
SamplesHuRef
Known GenesAGRN
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv987912
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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