A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712342



Internal ID136008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28266717..28266827hg38UCSC Ensembl
chr17:26593743..26593853hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560937
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712342
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001249


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