A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712795



Internal ID136461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35189716..35189767hg38UCSC Ensembl
chr17:33516735..33516786hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712795
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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