A curated catalogue of human genomic structural variation




Variant Details

Variant: essv84198



Internal ID11047459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121569278..121619614hg38UCSC Ensembl
Innerchr9:124331557..124381893hg19UCSC Ensembl
Innerchr9:123371378..123421714hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3850337
hg1950337
hg1850337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv29959
Supporting Variants
SamplesWATSON
Known GenesDAB2IP, MIR548AA1, MIR548D1
MethodOligo aCGH
AnalysisThe data were analyzed using the CGH Analytics software.
PlatformAgilent-014584 Human Genome 244K CGH Microarray (Alpha Test)
Comments
ReferenceWheeler_et_al_2008
Pubmed ID18421352
Accession Number(s)essv84198
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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