A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076351



Internal ID21985584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36879717..36879717hg38UCSC Ensembl
chr3:36921208..36921208hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546948
Samples
Known GenesTRANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076351
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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