A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639852



Internal ID21588157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105658380..105658380hg38UCSC Ensembl
chr9:108420661..108420661hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150887
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639852
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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