A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479124



Internal ID256659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21447873..21480507hg38UCSC Ensembl
chr9:21447872..21480506hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3832635
hg1932635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023430
Samples
Known GenesMIR31HG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479124
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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