A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6178192



Internal ID9155595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119358268..119358414hg38UCSC Ensembl
chr11:119228978..119229124hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662290
Supporting Variants
SamplesHG00479
Known GenesUSP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6178192
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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