A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14189732



Internal ID5580985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64783160..64787232hg38UCSC Ensembl
Innerchr11:64783210..64787182hg38UCSC Ensembl
Outerchr11:64783110..64787282hg38UCSC Ensembl
chr11:64550632..64554704hg19UCSC Ensembl
Innerchr11:64550682..64554654hg19UCSC Ensembl
Outerchr11:64550582..64554754hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384073
hg194073
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626666
Supporting Variants
SamplesNA19024
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14189732
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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