A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951881



Internal ID35282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94713503..94715360hg38UCSC Ensembl
chr4:95634654..95636511hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951881
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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