A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3153n54



Internal ID22771048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52846708..52848418hg38UCSC Ensembl
chr13:53420843..53422553hg19UCSC Ensembl
chr13:52318844..52320554hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381711
hg191711
hg181711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561675, nsv561677, nsv561678, nsv561674, nsv561676
Samples
Known GenesPCDH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3153n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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