A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8952289



Internal ID14295551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32412722..32412734hg38UCSC Ensembl
Innerchr11:32412713..32412743hg38UCSC Ensembl
Outerchr11:32412701..32412752hg38UCSC Ensembl
chr11:32434268..32434280hg19UCSC Ensembl
Innerchr11:32434259..32434289hg19UCSC Ensembl
Outerchr11:32434247..32434298hg19UCSC Ensembl
chr11:32390844..32390856hg18UCSC Ensembl
Innerchr11:32390865..32390835hg18UCSC Ensembl
Outerchr11:32390823..32390874hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3421146
Supporting Variants
SamplesNA18605
Known GenesWT1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8952289
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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