A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6338044



Internal ID9315447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33492041..33502797hg38UCSC Ensembl
chr2:33717108..33727864hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3810757
hg1910757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661374
Supporting Variants
SamplesNA18552
Known GenesRASGRP3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6338044
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