A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270235



Internal ID20479453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1356986..1356986hg38UCSC Ensembl
chr4:1350774..1350774hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758729
Supporting Variants
Samples
Known GenesUVSSA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270235
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