A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6283n54



Internal ID22774178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14933745..14938905hg38UCSC Ensembl
chr19:15044557..15049717hg19UCSC Ensembl
chr19:14905557..14910717hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg385161
hg195161
hg185161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv578689, nsv578692, nsv578695, nsv578688, nsv578687, nsv578690, nsv578683, nsv578691, nsv578694
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6283n54
Frequency
Sample Size17421
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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