A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492650



Internal ID269858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121553645..121553983hg38UCSC Ensembl
chr9:124315924..124316262hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492650
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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