A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003658



Internal ID70065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135013610..135014311hg38UCSC Ensembl
chr7:134698361..134699062hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478627
Supporting Variants
Samples
Known GenesAGBL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004371


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