A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955196



Internal ID37443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122610389..122610440hg38UCSC Ensembl
chr4:123531544..123531595hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395499
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955196
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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