A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528181



Internal ID21852538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46546467..46546519hg38UCSC Ensembl
chr2:46773606..46773658hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989417
Supporting Variants
Samples
Known GenesRHOQ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528181
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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