A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670445



Internal ID21618750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57525130..57525130hg38UCSC Ensembl
chr20:56100186..56100186hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117467
SamplesNA19650
Known GenesCTCFL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670445
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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