A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624058



Internal ID21816105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47305966..47305966hg38UCSC Ensembl
chr19:47809223..47809223hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624058
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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