A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1169e214



Internal ID22757063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19125893..19133892hg38UCSC Ensembl
chr6:19126124..19134123hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3608260, esv3608259
SamplesNA20529
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1169e214
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