A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14301563



Internal ID3508226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123808256..123811084hg38UCSC Ensembl
Innerchr11:123808261..123811080hg38UCSC Ensembl
Outerchr11:123808252..123811089hg38UCSC Ensembl
chr11:123678964..123681792hg19UCSC Ensembl
Innerchr11:123678969..123681788hg19UCSC Ensembl
Outerchr11:123678960..123681797hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382829
hg192829
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627966
Supporting Variants
SamplesHG03112
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14301563
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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