A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278812



Internal ID20488030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35260216..35260380hg38UCSC Ensembl
chr1:35725817..35725981hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278812
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