A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085998



Internal ID20653038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3412658..3416063hg38UCSC Ensembl
chr2:3416429..3419834hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg383406
hg193406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335664
Supporting Variants
Samples
Known GenesTRAPPC12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085998
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