A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641423



Internal ID6681508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82369046..82398572hg38UCSC Ensembl
chr17:80326922..80356448hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3829527
hg1929527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15767083
SamplesNA20519
Known GenesOGFOD3, UTS2R
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641423
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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