A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270797



Internal ID20480015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112342295..112342352hg38UCSC Ensembl
chr3:112061142..112061199hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747205
Supporting Variants
Samples
Known GenesCD200
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270797
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