A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5549627



Internal ID323263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232923222..232923377hg38UCSC Ensembl
chr1:233058968..233059123hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16898625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5549627
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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