A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634071



Internal ID21582376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26590404..26590404hg38UCSC Ensembl
chr8:26447920..26447920hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145555
SamplesHG01505
Known GenesDPYSL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634071
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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