A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628137



Internal ID6668281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133065549..133100485hg38UCSC Ensembl
chr11:132935444..132970380hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3834937
hg1934937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv237e214
Supporting Variantsessv14317796
SamplesHG01308
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628137
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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