A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758155



Internal ID20534015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188636925..188636925hg38UCSC Ensembl
chr3:188354713..188354713hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294787
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758155
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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