A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764408



Internal ID20540268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32963394..32963394hg38UCSC Ensembl
chr12:33116328..33116328hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764408
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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