A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959705



Internal ID40441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183661062..183661657hg38UCSC Ensembl
chr4:184582215..184582810hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467938
Supporting Variants
Samples
Known GenesTRAPPC11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959705
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.016084


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