A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139014



Internal ID21474555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33080381..33080381hg38UCSC Ensembl
chr3:33121873..33121873hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg384198
hg194198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622108
Supporting Variants
SamplesHG03371
Known GenesGLB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139014
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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