A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541898



Internal ID301761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67262327..67262327hg38UCSC Ensembl
chr2:67489459..67489459hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16914620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541898
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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