A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613765



Internal ID21805812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104764084..104764084hg38UCSC Ensembl
chr14:105230421..105230421hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613765
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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