A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982447



Internal ID20549487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66166484..66171091hg38UCSC Ensembl
chr10:67926242..67930849hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384608
hg194608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446263
Supporting Variants
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982447
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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