A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636066



Internal ID21828113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4364791..4364848hg38UCSC Ensembl
chr19:4364788..4364845hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044679
Supporting Variants
Samples
Known GenesSH3GL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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