A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7226n54



Internal ID22775121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:185580666..186002147hg38UCSC Ensembl
chr2:186445393..186866874hg19UCSC Ensembl
chr2:186153638..186575119hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38421482
hg19421482
hg18421482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv584021, nsv584019
Samples
Known GenesFSIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7226n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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