A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958402



Internal ID39585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169857282..169870932hg38UCSC Ensembl
chr4:170778433..170792083hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3813651
hg1913651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958402
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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