A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589785



Internal ID6977115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9790174..9806406hg38UCSC Ensembl
chr2:9930303..9946535hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3816233
hg1916233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10406809
SamplesHG02545
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589785
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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