A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471226



Internal ID22529117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33741376..33764625hg38UCSC Ensembl
chr15:34033577..34056826hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3823250
hg1923250
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863982
Supporting Variants
Samples
Known GenesRYR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471226
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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