A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11056n54



Internal ID19003232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167198269..167370176hg38UCSC Ensembl
chr6:167611757..167783664hg19UCSC Ensembl
chr6:167531747..167703654hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38171908
hg19171908
hg18171908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605340, nsv605341
Samples
Known GenesTTLL2, UNC93A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11056n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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