A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959568



Internal ID40351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179662256..179878730hg38UCSC Ensembl
chr4:180583409..180799883hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38216475
hg19216475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959568
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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