A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8674n54



Internal ID22776569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162412903..162534146hg38UCSC Ensembl
chr3:162130691..162251934hg19UCSC Ensembl
chr3:163613385..163734628hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38121244
hg19121244
hg18121244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592178, nsv592176, nsv592175, nsv592189
SamplesHGDP01304, NINDS_249
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8674n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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