A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630852



Internal ID21822899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63224..63224hg38UCSC Ensembl
chr3:197947785..197947785hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630852
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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