A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16928171



Internal ID19482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215177827..215177878hg38UCSC Ensembl
chr2:216042550..216042601hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16928171
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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