A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666436



Internal ID21614741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63942138..63942138hg38UCSC Ensembl
chr20:62573491..62573491hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117788
SamplesHG00732
Known GenesUCKL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666436
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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