A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14184859



Internal ID2722836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63558459..63582290hg38UCSC Ensembl
chr11:63325931..63349762hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3823832
hg1923832
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626647
Supporting Variants
SamplesHG02397
Known GenesHRASLS2, PLA2G16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14184859
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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