A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949928



Internal ID33966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46419614..46489397hg38UCSC Ensembl
chr4:46421631..46491414hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3869784
hg1969784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949928
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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