A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541866



Internal ID21866221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16094123..16094123hg38UCSC Ensembl
chr4:16095746..16095746hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6066119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541866
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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