A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968655



Internal ID46426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83020445..83020496hg38UCSC Ensembl
chr5:82316264..82316315hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413744
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968655
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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