A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946497



Internal ID31699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16986032..16986051hg38UCSC Ensembl
chr4:16987655..16987674hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946497
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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