A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988762



Internal ID6724732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79120561..79121330hg38UCSC Ensembl
Innerchr10:80880318..80881087hg19UCSC Ensembl
Innerchr10:80550324..80551093hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38770
hg19770
hg18770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587268
SamplesHuRef
Known GenesZMIZ1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988762
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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