A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093814



Internal ID21492177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49468614..49468614hg38UCSC Ensembl
chr13:50042750..50042750hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655255
Supporting Variants
SamplesNA19238
Known GenesSETDB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093814
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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