A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960101



Internal ID40704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170237253..170454416hg38UCSC Ensembl
chr4:171158404..171375567hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38217164
hg19217164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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