A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999868



Internal ID7082476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:30067657..30068741hg38UCSC Ensembl
Innerchr19:30558564..30559648hg19UCSC Ensembl
Innerchr19:35250404..35251488hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381085
hg191085
hg181085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587046
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999868
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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