A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711667



Internal ID135333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15084707..15085764hg38UCSC Ensembl
chr17:14988024..14989081hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523803
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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