A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597116



Internal ID6984430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98422519..98430280hg38UCSC Ensembl
chr3:98141363..98149124hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg387762
hg197762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv914e214
Supporting Variantsessv11074841
SamplesNA18565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597116
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