A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586615



Internal ID6711311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46409196..46409751hg38UCSC Ensembl
Innerchr10:47140000..47140555hg19UCSC Ensembl
Innerchr10:46560006..46560561hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38556
hg19556
hg18556
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995135
Supporting Variants
SamplesHuRef
Known GenesLINC00842
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586615
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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