A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120394



Internal ID21453725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148193866..148193866hg38UCSC Ensembl
chr3:147911653..147911653hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614578
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120394
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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