A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627737



Internal ID7014565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111344515..111347763hg38UCSC Ensembl
chr11:111215240..111218488hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383249
hg193249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14286902, essv14286903
SamplesNA19439, NA19431
Known GenesMIR4491
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627737
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer