A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626063



Internal ID7012897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40429641..40470893hg38UCSC Ensembl
Innerchr11:40429641..40470893hg38UCSC Ensembl
Outerchr11:40429141..40471393hg38UCSC Ensembl
chr11:40451191..40492443hg19UCSC Ensembl
Innerchr11:40451191..40492443hg19UCSC Ensembl
Outerchr11:40450691..40492943hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3841253
hg1941253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14103227
SamplesNA20758
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626063
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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