A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618625



Internal ID21810672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11307234..11308725hg38UCSC Ensembl
chr19:11417910..11419401hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381492
hg191492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052784
Supporting Variants
Samples
Known GenesTSPAN16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618625
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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