A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758919



Internal ID20534779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80759126..80759126hg38UCSC Ensembl
chr16:80793023..80793023hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290020
Samples
Known GenesCDYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758919
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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