A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099565



Internal ID20666605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187045..1987433hg38UCSC Ensembl
chr3:228728..2029117hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381800389
hg191800390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341880
Supporting Variants
Samples
Known GenesCHL1, CNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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