A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3443289



Internal ID15290242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26338063..26341152hg38UCSC Ensembl
Innerchr16:26339572..26340053hg38UCSC Ensembl
Outerchr16:26337953..26341272hg38UCSC Ensembl
chr16:26349384..26352473hg19UCSC Ensembl
Innerchr16:26350893..26351374hg19UCSC Ensembl
Outerchr16:26349274..26352593hg19UCSC Ensembl
chr16:26256885..26259974hg18UCSC Ensembl
Innerchr16:26258875..26258394hg18UCSC Ensembl
Outerchr16:26256775..26260094hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg383090
hg193090
hg183090
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808723
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3443289
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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