A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910465



Internal ID7746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31304589..31304589hg38UCSC Ensembl
chr2:31527455..31527455hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910465
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03238


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