A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610084



Internal ID21558389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4710902..4710902hg38UCSC Ensembl
chr1:4770962..4770962hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065965
SamplesHG03065
Known GenesAJAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610084
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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