A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068794



Internal ID21978027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170081258..170081258hg38UCSC Ensembl
chr3:169799046..169799046hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541903
Samples
Known GenesGPR160
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068794
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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