A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081068



Internal ID20648108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180399449..180419881hg38UCSC Ensembl
chr2:181264176..181284608hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg3820433
hg1920433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081068
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