A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389305



Internal ID21380440
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 StatusM
Merged Variants
Supporting Variantsnssv15704105
Samples
Known GenesGPR161
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389305
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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