A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627484



Internal ID7014313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100418907..100522989hg38UCSC Ensembl
chr11:100289638..100393720hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38104083
hg19104083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv227e214
Supporting Variantsessv14250886, essv14250888, essv14250887, essv14250885
SamplesHG01860, HG01801, HG01794, HG01805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627484
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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