A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956169



Internal ID38088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:116048225..116785496hg38UCSC Ensembl
chr4:116969381..117706652hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38737272
hg19737272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463768
Supporting Variants
Samples
Known GenesMIR1973
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956169
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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