A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663282



Internal ID21611587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:81045057..81045057hg38UCSC Ensembl
chr12:81438836..81438836hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096572
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663282
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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