A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752834



Internal ID20528694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67329730..67329730hg38UCSC Ensembl
chr11:67097201..67097201hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279100
Samples
Known GenesLOC100130987
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752834
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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