A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924691



Internal ID17207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:204021111..204021111hg38UCSC Ensembl
chr2:204885834..204885834hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924691
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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