A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205516



Internal ID20772556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14978355..15191598hg38UCSC Ensembl
chr2:15118479..15331722hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38213244
hg19213244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351554
Supporting Variants
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205516
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