A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11013n54



Internal ID20144437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162269602..162524507hg38UCSC Ensembl
chr6:162690634..162945539hg19UCSC Ensembl
chr6:162610624..162865529hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38254906
hg19254906
hg18254906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605146, nsv605124
SamplesHGDP01397
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11013n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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