A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603777



Internal ID21795824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100166152..100166152hg38UCSC Ensembl
chr14:100632489..100632489hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084789
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603777
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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