A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661137



Internal ID21609442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131367453..131367453hg38UCSC Ensembl
chr12:131851998..131851998hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17078103
SamplesHG00513
Known GenesLOC338797
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661137
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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