A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474495



Internal ID252153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35982136..35994308hg38UCSC Ensembl
chr9:35982133..35994305hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3812173
hg1912173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474495
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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