A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv882e214



Internal ID22756776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30226089..30305649hg38UCSC Ensembl
chr3:30267580..30347140hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3879561
hg1979561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595734, esv3595733
SamplesHG00956, NA18957, HG01805, HG00581
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv882e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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