A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978023



Internal ID22752958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105483405..105483405hg38UCSC Ensembl
chr13:106135754..106135754hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359851
Samples
Known GenesDAOA, DAOA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978023
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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