A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614071



Internal ID21806118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97817987..97817987hg38UCSC Ensembl
chr14:98284324..98284324hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614071
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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