A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474471



Internal ID252130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5794237..5794317hg38UCSC Ensembl
chr9:5794237..5794317hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020387
Samples
Known GenesERMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474471
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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