A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669677



Internal ID21617982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29074225..29074225hg38UCSC Ensembl
chr21:30446546..30446546hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118869
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669677
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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