A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661401



Internal ID21609706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73470429..73470429hg38UCSC Ensembl
chr12:73864209..73864209hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087111
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661401
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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