A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438716



Internal ID22104893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80663084..80663084hg38UCSC Ensembl
chr16:80696981..80696981hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767939
Samples
Known GenesCDYL2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438716
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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