A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14218982



Internal ID2436947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82359479..82414195hg38UCSC Ensembl
Innerchr11:82359487..82414187hg38UCSC Ensembl
Outerchr11:82359471..82414203hg38UCSC Ensembl
chr11:82070521..82125237hg19UCSC Ensembl
Innerchr11:82070529..82125229hg19UCSC Ensembl
Outerchr11:82070513..82125245hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3854717
hg1954717
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626996
Supporting Variants
SamplesHG02147
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14218982
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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