A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761737



Internal ID20537597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170081264..170081264hg38UCSC Ensembl
chr3:169799052..169799052hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271205
Samples
Known GenesGPR160
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761737
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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