A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464551



Internal ID22522438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10159183..10164308hg38UCSC Ensembl
chr12:10311782..10316907hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg385126
hg195126
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860133
Supporting Variants
Samples
Known GenesOLR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464551
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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