A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704105



Internal ID21376381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168119803..168122236hg38UCSC Ensembl
chr1:168089041..168091474hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382434
hg192434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389305
Supporting Variants
Samples
Known GenesGPR161
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704105
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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