A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6405n54



Internal ID22774300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33621607..33622360hg38UCSC Ensembl
chr19:34112513..34113266hg19UCSC Ensembl
chr19:38804353..38805106hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38754
hg19754
hg18754
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579330, nsv579331, nsv579332
Samples
Known GenesCHST8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6405n54
Frequency
Sample Size17421
Observed Gain34
Observed Loss5
Observed Complex0
Frequencyn/a


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