A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415913



Internal ID21073466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15248247..15251233hg38UCSC Ensembl
chr9:15248245..15251231hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382987
hg192987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230564
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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