A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618561



Internal ID21810608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80315769..80315769hg38UCSC Ensembl
chr17:78289569..78289569hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094694
Supporting Variants
Samples
Known GenesRNF213
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618561
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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