A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768204



Internal ID20544064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53097279..53097279hg38UCSC Ensembl
chr15:53389476..53389476hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768204
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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