A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671033



Internal ID21619338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21155628..21155628hg38UCSC Ensembl
chr20:21136269..21136269hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116461
SamplesHG02587
Known GenesPLK1S1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671033
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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