A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666979



Internal ID21615285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41987525..41987525hg38UCSC Ensembl
chr21:43407634..43407634hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118635
SamplesNA12329
Known GenesZBTB21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666979
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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