A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1406e214



Internal ID22757300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85366203..85379406hg38UCSC Ensembl
chr8:86278432..86291635hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3813204
hg1913204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3617875, esv3617874
SamplesHG02166, HG00684, NA18608
Known GenesCA1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1406e214
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