A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633563



Internal ID21825610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67251612..67251612hg38UCSC Ensembl
chr17:65247728..65247728hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633563
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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