A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959445



Internal ID40271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175568610..175621774hg38UCSC Ensembl
chr4:176489761..176542925hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3853165
hg1953165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455123
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959445
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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