A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960177



Internal ID40758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171041966..171042017hg38UCSC Ensembl
chr4:171963117..171963168hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405922
Supporting Variants
Samples
Known GenesLOC100506122
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960177
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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