A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998868



Internal ID66819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79667075..79667400hg38UCSC Ensembl
chr7:79296391..79296716hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998868
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