A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993388



Internal ID63049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12142242..12182621hg38UCSC Ensembl
chr7:12181868..12222247hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3840380
hg1940380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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