A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764365



Internal ID20540225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102405251..102405251hg38UCSC Ensembl
chr12:102799029..102799029hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293796
Samples
Known GenesIGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764365
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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