A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946100



Internal ID31418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:234535..404755hg38UCSC Ensembl
chr4:228324..398544hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38170221
hg19170221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139642
Supporting Variants
Samples
Known GenesZNF141, ZNF732, ZNF876P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946100
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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