A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625990



Internal ID7012824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37745699..37823206hg38UCSC Ensembl
chr11:37767249..37844756hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3877508
hg1977508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv192e214
Supporting Variantsessv14095016, essv14095018, essv14095019, essv14095017
SamplesHG01402, NA20863, HG02221, HG02314
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625990
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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