A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626114



Internal ID7012948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42422105..42498476hg38UCSC Ensembl
chr11:42443655..42520026hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3876372
hg1976372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv194e214
Supporting Variantsessv14109699, essv14109697, essv14109698
SamplesHG01031, HG02075, HG03598
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626114
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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