A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409899



Internal ID189219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16709869..16709920hg38UCSC Ensembl
chr9:16709867..16709918hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021648
Samples
Known GenesBNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409899
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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