A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7734077



Internal ID13873748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138451969..138451970hg38UCSC Ensembl
Outerchr3:138451778..138452161hg38UCSC Ensembl
Innerchr3:138170811..138170812hg19UCSC Ensembl
Outerchr3:138170620..138171003hg19UCSC Ensembl
Innerchr3:139653502..139653501hg18UCSC Ensembl
Outerchr3:139653310..139653693hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38384
hg19384
hg18384
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302999
Supporting Variants
SamplesNA18517
Known GenesESYT3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7734077
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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