A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv891e214



Internal ID22756785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53970892..54001502hg38UCSC Ensembl
chr3:54004919..54035529hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3830611
hg1930611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596174, esv3596175
SamplesNA12283, HG03762, HG01198
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv891e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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