A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084668



Internal ID20651708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:204458520..204472728hg38UCSC Ensembl
chr2:205323243..205337451hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3814209
hg1914209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084668
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