A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543899



Internal ID21868254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169167961..169167961hg38UCSC Ensembl
chr3:168885749..168885749hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064197
Supporting Variants
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543899
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