A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590292



Internal ID6630579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33491880..33502655hg38UCSC Ensembl
Innerchr2:33491929..33502607hg38UCSC Ensembl
Outerchr2:33491832..33502704hg38UCSC Ensembl
chr2:33716947..33727722hg19UCSC Ensembl
Innerchr2:33716996..33727674hg19UCSC Ensembl
Outerchr2:33716899..33727771hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3810776
hg1910776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv684e214
Supporting Variantsessv10451264
SamplesNA18552
Known GenesRASGRP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590292
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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