A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537259



Internal ID312584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32883288..32883288hg38UCSC Ensembl
chr9:32883286..32883286hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537259
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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