A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615195



Internal ID21563500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33953063..33953063hg38UCSC Ensembl
chr3:33994555..33994555hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135803
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615195
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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