A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057981



Internal ID106500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9080960..9081011hg38UCSC Ensembl
chr2:9221089..9221140hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408002
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057981
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007805


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