A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5906167



Internal ID9712426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109525899..109530188hg38UCSC Ensembl
chr11:109396625..109400914hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384290
hg194290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676683
Supporting Variants
SamplesNA19463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5906167
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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