A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473938



Internal ID251618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94280000..94576600hg38UCSC Ensembl
chr9:97042282..97338882hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38296601
hg19296601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025750
Samples
Known GenesFBP2, HIATL1, LOC100132077, NUTM2F, ZNF169
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473938
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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