A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3359n54



Internal ID22771254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99086152..99087408hg38UCSC Ensembl
chr13:99738406..99739662hg19UCSC Ensembl
chr13:98536407..98537663hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381257
hg191257
hg181257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562930, nsv562928, nsv562931
Samples
Known GenesDOCK9, DOCK9-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3359n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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