A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491220



Internal ID268463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3835768..3836569hg38UCSC Ensembl
chr9:3835768..3836569hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017826
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491220
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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