A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475722



Internal ID253357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11347313..11623109hg38UCSC Ensembl
chr9:11347313..11623109hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38275797
hg19275797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475722
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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