A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120992



Internal ID21508110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94043620..94043620hg38UCSC Ensembl
chr3:93762464..93762464hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624213
Supporting Variants
SamplesNA20509
Known GenesARL13B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120992
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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