A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623589



Internal ID21815636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49231786..49234150hg38UCSC Ensembl
chr19:49735043..49737407hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382365
hg192365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623589
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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