A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622099



Internal ID21570404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99193503..99193503hg38UCSC Ensembl
chr3:98912347..98912347hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128492
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622099
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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