A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711661



Internal ID135327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15055805..15068535hg38UCSC Ensembl
chr17:14959122..14971852hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3812731
hg1912731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711661
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