A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542029



Internal ID316519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13424322..13424322hg38UCSC Ensembl
chr9:13424321..13424321hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020523
Samples
Known GenesFLJ41200
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542029
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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