A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752511



Internal ID20528371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106589112..106589112hg38UCSC Ensembl
chr6:107036987..107036987hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295329
Samples
Known GenesRTN4IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752511
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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