A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080179



Internal ID20647219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162253365..162254089hg38UCSC Ensembl
chr2:163109875..163110599hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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