A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921093



Internal ID22696316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123082633..123082730hg38UCSC Ensembl
chr9:125844912..125845009hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430733
Samples
Known GenesRABGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921093
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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