A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622830



Internal ID21571135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176326313..176326313hg38UCSC Ensembl
chr3:176044101..176044101hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120456
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622830
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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