A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv679e214



Internal ID22756573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20904452..20933028hg38UCSC Ensembl
chr2:21104212..21132788hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3828577
hg1928577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3590003, esv3590004
SamplesHG01080, HG01205, HG01086
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv679e214
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