A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959447



Internal ID40273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175575633..175628170hg38UCSC Ensembl
chr4:176496784..176549321hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3852538
hg1952538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959447
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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