A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712314



Internal ID135980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27826353..27826356hg38UCSC Ensembl
chr17:26153379..26153382hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38907
hg19907
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712314
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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