A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9936n54



Internal ID20143360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93584115..93585189hg38UCSC Ensembl
chr5:92919821..92920895hg19UCSC Ensembl
chr5:92945577..92946651hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381075
hg191075
hg181075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598948, nsv598946, nsv598947, nsv598945
Samples
Known GenesNR2F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9936n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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