A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541449



Internal ID298763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89968678..89968678hg38UCSC Ensembl
chr1:90434237..90434237hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541449
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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