A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926426



Internal ID18342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237485007..237485056hg38UCSC Ensembl
chr2:238393650..238393699hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926426
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.040456


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