A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672459



Internal ID21620764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29386200..29386200hg38UCSC Ensembl
chr21:30758520..30758520hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119260
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672459
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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