A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3353568



Internal ID15200549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64463714..64468612hg38UCSC Ensembl
Innerchr9:64464714..64467612hg38UCSC Ensembl
Outerchr9:64462714..64469612hg38UCSC Ensembl
chr9:69476132..69481030hg19UCSC Ensembl
Innerchr9:69477132..69480030hg19UCSC Ensembl
Outerchr9:69475132..69482030hg19UCSC Ensembl
chr9:68765952..68770850hg18UCSC Ensembl
Innerchr9:68766952..68769850hg18UCSC Ensembl
Outerchr9:68764952..68771850hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg384899
hg194899
hg184899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697219
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3353568
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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