A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756759



Internal ID20532619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189214954..189214954hg38UCSC Ensembl
chr3:188932743..188932743hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266841
Samples
Known GenesTPRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756759
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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