A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704339



Internal ID21376615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9640314..9643446hg38UCSC Ensembl
chr8:9497824..9500956hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383133
hg193133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388742
Supporting Variants
Samples
Known GenesTNKS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704339
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.117816


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