A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14320192



Internal ID2030041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134287846..134329219hg38UCSC Ensembl
chr11:134157740..134199113hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3841374
hg1941374
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628166
Supporting Variants
SamplesHG01864
Known GenesGLB1L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14320192
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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