A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767274



Internal ID20543134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57480248..57480248hg38UCSC Ensembl
chr15:57772446..57772446hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264491
Samples
Known GenesCGNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767274
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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