A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627653



Internal ID7014481
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv230e214
Supporting Variantsessv14276848, essv14276847, essv14276846
SamplesHG00238, NA19328, NA19468
Known GenesSLC35F2, SLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627653
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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