A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14189733



Internal ID4191549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65009442..65019708hg38UCSC Ensembl
chr11:64776914..64787180hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3810267
hg1910267
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626667
Supporting Variants
SamplesHG01921
Known GenesARL2, ARL2-SNX15, MIR6879
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14189733
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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