A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003390



Internal ID69880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140480159..140480479hg38UCSC Ensembl
chr7:140179959..140180279hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483322
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003390
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