A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588666



Internal ID21537229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36736752..36736805hg38UCSC Ensembl
chr21:38109053..38109106hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119090
SamplesHG03486
Known GenesSIM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588666
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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