A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485799



Internal ID263181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16804966..16818337hg38UCSC Ensembl
chr9:16804964..16818335hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3813372
hg1913372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021652
Samples
Known GenesBNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485799
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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