A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14276181



Internal ID4427007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107365263..107376158hg38UCSC Ensembl
Innerchr11:107365763..107375658hg38UCSC Ensembl
Outerchr11:107364263..107377158hg38UCSC Ensembl
chr11:107235989..107246884hg19UCSC Ensembl
Innerchr11:107236489..107246384hg19UCSC Ensembl
Outerchr11:107234989..107247884hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810896
hg1910896
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627647
Supporting Variants
SamplesHG03941
Known GenesCWF19L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14276181
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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