A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627872



Internal ID6668016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118502100..118536457hg38UCSC Ensembl
chr11:118372815..118407172hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3834358
hg1934358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14293207
SamplesHG00326
Known GenesKMT2A, TMEM25, TTC36
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627872
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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