A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5575612



Internal ID9098461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20904475..20931372hg38UCSC Ensembl
chr2:21104235..21131132hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3826898
hg1926898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668566
Supporting Variants
SamplesHG01080
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5575612
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