A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762181



Internal ID20538041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188602121..188602121hg38UCSC Ensembl
chr3:188319909..188319909hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260965
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762181
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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