A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3374413



Internal ID14874675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14185373..14185380hg38UCSC Ensembl
Innerchr3:14185368..14185385hg38UCSC Ensembl
Outerchr3:14185361..14185392hg38UCSC Ensembl
chr3:14226873..14226880hg19UCSC Ensembl
Innerchr3:14226868..14226885hg19UCSC Ensembl
Outerchr3:14226861..14226892hg19UCSC Ensembl
chr3:14201877..14201884hg18UCSC Ensembl
Innerchr3:14201889..14201872hg18UCSC Ensembl
Outerchr3:14201865..14201896hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3859
hg1959
hg1859
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864107
SamplesNA12005
Known GenesLSM3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3374413
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