A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287928



Internal ID20497146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100412712..100412712hg38UCSC Ensembl
chr1:100878268..100878268hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767586
Supporting Variants
Samples
Known GenesCDC14A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287928
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