A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000689



Internal ID68030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98734022..98738071hg38UCSC Ensembl
chr7:98363334..98367383hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg384050
hg194050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484795
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000689
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