A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627379



Internal ID7014208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96411732..96429118hg38UCSC Ensembl
chr11:96144896..96162282hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3817387
hg1917387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14245179, essv14245180, essv14245181
SamplesNA19648, NA20518, HG00554
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627379
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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