A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946140



Internal ID31445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:442134..503546hg38UCSC Ensembl
chr4:435923..497335hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3861413
hg1961413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451505
Supporting Variants
Samples
Known GenesABCA11P, PIGG, ZNF721
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946140
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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