A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704426



Internal ID21376702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61033314..61033462hg38UCSC Ensembl
chr8:61945873..61946021hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388821
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704426
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.456897


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