A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14092097



Internal ID3236211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37315969..37354612hg38UCSC Ensembl
chr11:37337519..37376162hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3838644
hg1938644
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625975
Supporting Variants
SamplesHG02852
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14092097
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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