A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8228n54



Internal ID22776123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13029299..13094075hg38UCSC Ensembl
chr3:13070799..13135575hg19UCSC Ensembl
chr3:13045799..13110575hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3864777
hg1964777
hg1864777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589722, nsv589723, nsv589724
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8228n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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