A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5545041



Internal ID319122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196460093..196460099hg38UCSC Ensembl
chr2:197324817..197324823hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16923387
Samples
Known GenesHECW2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5545041
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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