A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663672



Internal ID21611977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4105959..4105959hg38UCSC Ensembl
chr12:4215125..4215125hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096656
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663672
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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