A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106730



Internal ID20673770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94535504..94539565hg38UCSC Ensembl
chr3:94254348..94258409hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg384062
hg194062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370196
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106730
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