A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290197



Internal ID20499415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196470073..196470147hg38UCSC Ensembl
chr3:196196944..196197018hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749538
Supporting Variants
Samples
Known GenesRNF168
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290197
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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