A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3593620



Internal ID6980943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:184492826..184543656hg38UCSC Ensembl
chr2:185357553..185408383hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3850831
hg1950831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10789743
SamplesNA19350
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3593620
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