A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090627



Internal ID4413162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36066286..36087625hg38UCSC Ensembl
chr11:36087836..36109175hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3821340
hg1921340
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625946
Supporting Variants
SamplesHG03928
Known GenesLDLRAD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090627
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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