A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419026



Internal ID198174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70177511..70177562hg38UCSC Ensembl
chr17:68173652..68173703hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714321
Samples
Known GenesKCNJ2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419026
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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