A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959877



Internal ID40565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165069827..165070017hg38UCSC Ensembl
chr4:165990979..165991169hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462418
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959877
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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