A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289104



Internal ID20498322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40683416..40683547hg38UCSC Ensembl
chr15:40975614..40975745hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730880
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289104
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