A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16913652



Internal ID9840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46548771..46563099hg38UCSC Ensembl
chr2:46775910..46790238hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3814329
hg1914329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449463
Supporting Variants
Samples
Known GenesRHOQ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16913652
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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