A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460620



Internal ID22518503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133243526..133251514hg38UCSC Ensembl
chr12:133820112..133828100hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg387989
hg197989
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864009
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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