A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6406n54



Internal ID20139830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33621658..33622360hg38UCSC Ensembl
chr19:34112564..34113266hg19UCSC Ensembl
chr19:38804404..38805106hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38703
hg19703
hg18703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579336, nsv579338, nsv579335, nsv579337, nsv579333, nsv579334
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6406n54
Frequency
Sample Size17421
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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