A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633774



Internal ID21582079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32885017..32885017hg38UCSC Ensembl
chr8:32742535..32742535hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140176
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633774
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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