A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670191



Internal ID21618498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36054625..36054625hg38UCSC Ensembl
chr21:37426923..37426923hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118559
SamplesHG02587
Known GenesSETD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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