A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14114423



Internal ID1918519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43860473..43861883hg38UCSC Ensembl
Innerchr11:43860511..43861846hg38UCSC Ensembl
Outerchr11:43860436..43861921hg38UCSC Ensembl
chr11:43882023..43883433hg19UCSC Ensembl
Innerchr11:43882061..43883396hg19UCSC Ensembl
Outerchr11:43881986..43883471hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626154
Supporting Variants
SamplesHG01796
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14114423
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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