A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958993



Internal ID39965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160261175..160263755hg38UCSC Ensembl
chr4:161182327..161184907hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382581
hg192581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958993
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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