A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704462



Internal ID21376738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86176020..86181514hg38UCSC Ensembl
chr8:87188249..87193743hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg385495
hg195495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388853
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704462
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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