A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3381666



Internal ID15228638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90161850..90163148hg38UCSC Ensembl
Innerchr9:90162148..90162850hg38UCSC Ensembl
Outerchr9:90160850..90164148hg38UCSC Ensembl
chr9:92924132..92925430hg19UCSC Ensembl
Innerchr9:92924430..92925132hg19UCSC Ensembl
Outerchr9:92923132..92926430hg19UCSC Ensembl
chr9:91963952..91965250hg18UCSC Ensembl
Innerchr9:91964952..91964250hg18UCSC Ensembl
Outerchr9:91962952..91966250hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4474e59
Supporting Variantsessv8697418
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3381666
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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