A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205399



Internal ID20772439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:188306280..188334355hg38UCSC Ensembl
chr2:189171007..189199082hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3828076
hg1928076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347439
Supporting Variants
Samples
Known GenesGULP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer