A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5442353



Internal ID8784838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3044654..3045523hg38UCSC Ensembl
chr11:3065884..3066753hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668116
Supporting Variants
SamplesHG00187
Known GenesCARS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5442353
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