A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620374



Internal ID7007245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35229813..35233300hg38UCSC Ensembl
chr9:35229810..35233297hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383488
hg193488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13459357, essv13459358, essv13459356
SamplesNA19099, NA19310, HG00329
Known GenesUNC13B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620374
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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