A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081209



Internal ID20648249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:193006028..193227114hg38UCSC Ensembl
chr2:193870754..194091840hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38221087
hg19221087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081209
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