A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587452



Internal ID21779495
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 StatusS
Merged Variantsnsv6013018
Supporting Variants
Samples
Known GenesRABGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587452
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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