A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760383



Internal ID20536243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3876665..3876665hg38UCSC Ensembl
chr9:3876665..3876665hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285081
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760383
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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