A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920557



Internal ID22695780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98461209..98464553hg38UCSC Ensembl
chr9:101223491..101226835hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383345
hg193345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440282
Samples
Known GenesGABBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920557
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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