A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628167



Internal ID6668311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134287846..134329219hg38UCSC Ensembl
chr11:134157740..134199113hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3841374
hg1941374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14320195, essv14320203, essv14320200, essv14320196, essv14320202, essv14320201, essv14320199, essv14320198, essv14320197
SamplesHG01815, HG01066, NA18639, NA18534, HG02259, NA18533, NA19037, HG00607, HG01861
Known GenesGLB1L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628167
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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