A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293796



Internal ID20503014
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 StatusS
Merged Variantsnsv4764365
Supporting Variants
Samples
Known GenesIGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293796
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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