A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1136n54



Internal ID20134560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52256302..52257509hg38UCSC Ensembl
chr10:54016062..54017269hg19UCSC Ensembl
chr10:53686068..53687275hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381208
hg191208
hg181208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550890, nsv550882, nsv550881, nsv550891, nsv550883
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1136n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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