A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927659



Internal ID19148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191667930..191667937hg38UCSC Ensembl
chr2:192532656..192532663hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541337
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.047017


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