A curated catalogue of human genomic structural variation




Variant Details

Variant: esv995135



Internal ID6731085
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 Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586615
SamplesHuRef
Known GenesLINC00842
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv995135
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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