A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093304



Internal ID20660344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108322394..108323140hg38UCSC Ensembl
chr3:108041241..108041987hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357166
Supporting Variants
Samples
Known GenesHHLA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093304
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