A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735224



Internal ID158890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170810389..170815801hg38UCSC Ensembl
chr4:171731540..171736952hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg385413
hg195413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735224
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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