A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv865e214



Internal ID20122288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4092194..4142900hg38UCSC Ensembl
chr3:4133878..4184584hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3850707
hg1950707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595085, esv3595084
SamplesHG00766, NA18877, HG02600, HG03518, NA19098, HG03199, HG01046, NA19385, HG03814, HG02427, NA18557, NA19327, NA20903, HG04054, HG02256, NA20542, HG03934, NA19019, HG03433, HG00728, NA20502, HG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv865e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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