A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724773



Internal ID148439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55661043..55661143hg38UCSC Ensembl
chr17:53738404..53738504hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724773
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009835


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