A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696812



Internal ID15059531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64461257..64470879hg38UCSC Ensembl
Innerchr9:64462257..64469867hg38UCSC Ensembl
Outerchr9:64460257..64471893hg38UCSC Ensembl
chr9:43026056..43035654hg19UCSC Ensembl
Innerchr9:43027056..43034654hg19UCSC Ensembl
Outerchr9:43025056..43036654hg19UCSC Ensembl
chr9:43016052..43025650hg18UCSC Ensembl
Innerchr9:43017052..43024650hg18UCSC Ensembl
Outerchr9:43015052..43026650hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg389623
hg199599
hg189599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3332978
Supporting Variants
SamplesNA19239
Known GenesFAM95B1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696812
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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