A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11010n54



Internal ID20144434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162171775..162270386hg38UCSC Ensembl
chr6:162592807..162691418hg19UCSC Ensembl
chr6:162512797..162611408hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3898612
hg1998612
hg1898612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605110, nsv605115
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11010n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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