A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260266



Internal ID20469484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122726865..122726865hg38UCSC Ensembl
chr3:122445712..122445712hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763420
Supporting Variants
Samples
Known GenesPARP14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260266
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