A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197003



Internal ID20764043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51088780..51105059hg38UCSC Ensembl
chr17:49166141..49182420hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3816280
hg1916280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526765
Supporting Variants
Samples
Known GenesSPAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197003
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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