A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765325



Internal ID20541185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105502118..105502118hg38UCSC Ensembl
chr14:105968455..105968455hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765325
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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