A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490467



Internal ID267724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126016062..126020537hg38UCSC Ensembl
chr9:128778341..128782816hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384476
hg194476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490467
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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