A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696761



Internal ID13731683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65145877..65160565hg38UCSC Ensembl
Innerchr9:65146877..65159565hg38UCSC Ensembl
Outerchr9:64639682..65161569hg38UCSC Ensembl
chr9:42841556..42856254hg19UCSC Ensembl
Innerchr9:42842556..42855254hg19UCSC Ensembl
Outerchr9:42840556..42857254hg19UCSC Ensembl
chr9:42831552..42846250hg18UCSC Ensembl
Innerchr9:42832552..42845250hg18UCSC Ensembl
Outerchr9:42830552..42847250hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3814689
hg1914699
hg1814699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3407644
Supporting Variants
SamplesNA12892
Known GenesLOC286297
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696761
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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