A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926405



Internal ID18329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237157822..237157861hg38UCSC Ensembl
chr2:238066465..238066504hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553589
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926405
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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