A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629011



Internal ID21821058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45798838..45798838hg38UCSC Ensembl
chr19:46302096..46302096hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381639
hg191639
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104543
Supporting Variants
Samples
Known GenesRSPH6A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629011
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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