A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959348



Internal ID40206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174383668..174401404hg38UCSC Ensembl
chr4:175304819..175322555hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3817737
hg1917737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959348
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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