A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3365168



Internal ID15212145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10001..11850hg38UCSC Ensembl
Innerchr5:10850..10952hg38UCSC Ensembl
chr5:10001..11850hg19UCSC Ensembl
Innerchr5:10850..10952hg19UCSC Ensembl
chr5:62952..64850hg18UCSC Ensembl
Innerchr5:63952..63850hg18UCSC Ensembl
Outerchr5:61952..65850hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381850
hg191850
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3178e59
Supporting Variantsessv8694834
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3365168
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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