A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437699



Internal ID22103879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4344182..4344182hg38UCSC Ensembl
chr16:4394183..4394183hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381673
hg191673
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759926
Samples
Known GenesCORO7-PAM16, PAM16
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437699
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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