A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438662



Internal ID22104842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3876677..3876677hg38UCSC Ensembl
chr9:3876677..3876677hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760249
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438662
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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