A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089459



Internal ID20656499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61167302..61169052hg38UCSC Ensembl
chr2:61394437..61396187hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381751
hg191751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351497
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089459
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