A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578966



Internal ID21527441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121365541..121365605hg38UCSC Ensembl
chr4:122286696..122286760hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121985
SamplesHG00732
Known GenesQRFPR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578966
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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