A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098971



Internal ID20666011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17615632..17621566hg38UCSC Ensembl
chr3:17657124..17663058hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385935
hg195935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373029
Supporting Variants
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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