A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632918



Internal ID21824965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28224008..28224008hg38UCSC Ensembl
chr17:26551034..26551034hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087948
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632918
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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