A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8362n54



Internal ID22776257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66500053..66501284hg38UCSC Ensembl
chr3:66550477..66551708hg19UCSC Ensembl
chr3:66633167..66634398hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381232
hg191232
hg181232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590551, nsv590555, nsv590552
Samples
Known GenesLRIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8362n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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