A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052804



Internal ID20619844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:164979842..164982812hg38UCSC Ensembl
chr1:164949079..164952049hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382971
hg192971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052804
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