A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668909



Internal ID21617214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37823947..37823947hg38UCSC Ensembl
chr21:39196249..39196249hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119309
SamplesHG00731
Known GenesKCNJ6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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