A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600260



Internal ID21792307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100345050..100345050hg38UCSC Ensembl
chr14:100811387..100811387hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084221
Supporting Variants
Samples
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600260
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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