A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3331n54



Internal ID20136755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97433070..97434574hg38UCSC Ensembl
chr13:98085324..98086828hg19UCSC Ensembl
chr13:96883325..96884829hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381505
hg191505
hg181505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562800, nsv562797, nsv562798, nsv562796, nsv562799
Samples
Known GenesRAP2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3331n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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