A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627318



Internal ID7014148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94339470..94354013hg38UCSC Ensembl
chr11:94072636..94087179hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3814544
hg1914544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14241829, essv14241830, essv14241821, essv14241828, essv14241827, essv14241824, essv14241825, essv14241822, essv14241823, essv14241820, essv14241826
SamplesHG01066, NA20586, NA20819, HG01619, NA11893, NA20538, HG04006, NA20807, HG01431, HG01756, NA20827
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627318
Frequency
Sample Size2504
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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