A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3332n54



Internal ID22771227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97446270..97456107hg38UCSC Ensembl
chr13:98098524..98108361hg19UCSC Ensembl
chr13:96896525..96906362hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg389838
hg199838
hg189838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562805, nsv562803, nsv562804, nsv562802
Samples
Known GenesRAP2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3332n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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