A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6394n54



Internal ID22774289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29566638..29567903hg38UCSC Ensembl
chr19:30057545..30058810hg19UCSC Ensembl
chr19:34749385..34750650hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381266
hg191266
hg181266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579278, nsv579279, nsv579277, nsv579276
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6394n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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