A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670918



Internal ID21619223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32123203..32123203hg38UCSC Ensembl
chr20:30711006..30711006hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115973
SamplesHG02011
Known GenesTM9SF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670918
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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