A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999415



Internal ID6735340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26429654..26430140hg38UCSC Ensembl
Innerchr22:26825620..26826106hg19UCSC Ensembl
Innerchr22:25155620..25156106hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38487
hg19487
hg18487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587015
SamplesHuRef
Known GenesASPHD2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999415
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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