A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626580



Internal ID7013412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61437001..61457837hg38UCSC Ensembl
chr11:61204473..61225309hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3820837
hg1920837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14178495
SamplesNA20775
Known GenesSDHAF2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626580
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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