A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295268



Internal ID20504486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37812576..37812656hg38UCSC Ensembl
chr15:38104777..38104857hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295268
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