A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959903



Internal ID40580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165483708..165483806hg38UCSC Ensembl
chr4:166404860..166404958hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462541
Supporting Variants
Samples
Known GenesCPE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959903
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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