A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765608



Internal ID20541468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32412722..32412722hg38UCSC Ensembl
chr11:32434268..32434268hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295639
Samples
Known GenesWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765608
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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