A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1460e214



Internal ID22757354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24702466..24760660hg38UCSC Ensembl
chr9:24702464..24760658hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3858195
hg1958195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3620045, esv3620046
SamplesHG00358, HG01136, HG00343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1460e214
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