A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926082



Internal ID18128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223141853..223141858hg38UCSC Ensembl
chr2:224006571..224006576hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg386014
hg196014
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926082
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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