A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612322



Internal ID21560627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117326382..117326382hg38UCSC Ensembl
chr1:117869004..117869004hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059801
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612322
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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