A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477566



Internal ID255143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118254610..118256338hg38UCSC Ensembl
chr9:121016888..121018616hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg381729
hg191729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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