A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12024n54



Internal ID22779919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16103682..16163959hg38UCSC Ensembl
chr8:15961191..16021468hg19UCSC Ensembl
chr8:16005562..16065839hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3860278
hg1960278
hg1860278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610595, nsv610596, nsv610593
Samples
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12024n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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