A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662608



Internal ID21610913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41774642..41774642hg38UCSC Ensembl
chr12:42168444..42168444hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089103
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662608
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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