A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17721229



Internal ID144895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9510429..9510566hg38UCSC Ensembl
chr19:9621105..9621242hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17721229
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