A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053458



Internal ID21962691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17593099..17593483hg38UCSC Ensembl
chr19:17703908..17704292hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053458
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