A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669161



Internal ID21617466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36609156..36609156hg38UCSC Ensembl
chr20:35237559..35237559hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116883
SamplesHG00732
Known GenesC20orf24, TGIF2-C20orf24
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669161
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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