A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537986



Internal ID21862341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125067484..125067484hg38UCSC Ensembl
chr3:124786328..124786328hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537986
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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