A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3425981



Internal ID14926252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66846048..66847846hg38UCSC Ensembl
Innerchr16:66846846..66847048hg38UCSC Ensembl
Outerchr16:66845048..66848846hg38UCSC Ensembl
chr16:66879951..66881749hg19UCSC Ensembl
Innerchr16:66880749..66880951hg19UCSC Ensembl
Outerchr16:66878951..66882749hg19UCSC Ensembl
chr16:65437452..65439250hg18UCSC Ensembl
Innerchr16:65438452..65438250hg18UCSC Ensembl
Outerchr16:65436452..65440250hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8690408
SamplesNA19239
Known GenesCA7
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3425981
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