A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14276848



Internal ID4278664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107682939..107801382hg38UCSC Ensembl
chr11:107553665..107672108hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38118444
hg19118444
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627653
Supporting Variants
SamplesNA19468
Known GenesSLC35F2, SLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14276848
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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