A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263620



Internal ID20472838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5622730..5622730hg38UCSC Ensembl
chr17:5526050..5526050hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263620
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