A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484677



Internal ID262088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31009193..31029393hg38UCSC Ensembl
chr9:31009191..31029391hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3820201
hg1920201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484677
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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