A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635191



Internal ID21583496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9950380..9950380hg38UCSC Ensembl
chr8:9807890..9807890hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144352
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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