A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866903



Internal ID22641838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:252601..255924hg38UCSC Ensembl
chr12:361767..365090hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg383324
hg193324
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461959
Samples
Known GenesSLC6A13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866903
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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