A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754962



Internal ID20530822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92428626..92428626hg38UCSC Ensembl
chr12:92822402..92822402hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295673
Samples
Known GenesCLLU1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754962
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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