A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640273



Internal ID7027048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22696461..22742174hg38UCSC Ensembl
chr17:22195788..22241501hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg3845714
hg1945714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15652838, essv15652843, essv15652835, essv15652853, essv15652842, essv15652848, essv15652844, essv15652847, essv15652846, essv15652849, essv15652845, essv15652836, essv15652832, essv15652852, essv15652837, essv15652833, essv15652841, essv15652834, essv15652839, essv15652850, essv15652851, essv15652840
SamplesNA20882, NA20853, HG03965, HG04018, HG03895, NA20863, HG04156, NA21135, HG03757, NA20850, HG02489, NA20910, HG04106, HG03693, HG00436, HG03900, HG03771, NA20866, HG03672, HG03848, HG04090, HG03886
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640273
Frequency
Sample Size2504
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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