A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8519n54



Internal ID22776414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119632551..119635586hg38UCSC Ensembl
chr3:119351398..119354433hg19UCSC Ensembl
chr3:120834088..120837123hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383036
hg193036
hg183036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591369, nsv591368, nsv591370, nsv591374, nsv591371, nsv591373, nsv591367, nsv591366, nsv591372
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8519n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss59
Observed Complex0
Frequencyn/a


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