A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615599



Internal ID21563904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111502086..111502086hg38UCSC Ensembl
chr1:112044708..112044708hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059933
SamplesNA18534
Known GenesADORA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615599
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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