A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669896



Internal ID21618201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33344481..33344481hg38UCSC Ensembl
chr21:34716787..34716787hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119077
SamplesNA19650
Known GenesIFNAR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669896
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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