A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17058689



Internal ID106990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53577048..53581383hg38UCSC Ensembl
chr12:53970832..53975167hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg384336
hg194336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511438
Supporting Variants
Samples
Known GenesATF7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17058689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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