A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294311



Internal ID20503529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38156966..38157051hg38UCSC Ensembl
chr8:38014484..38014569hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294311
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