A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285528



Internal ID20494746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89543839..89543839hg38UCSC Ensembl
chr12:89937616..89937616hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751528
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285528
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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