A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720956



Internal ID144622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6689302..6689362hg38UCSC Ensembl
chr19:6689313..6689373hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5518068
Supporting Variants
Samples
Known GenesC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720956
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009844


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