A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612362



Internal ID21560667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31176667..31176667hg38UCSC Ensembl
chr1:31649514..31649514hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064593
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612362
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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