A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281984



Internal ID20491202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95355491..95355491hg38UCSC Ensembl
chr12:95749267..95749267hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281984
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer