A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630884



Internal ID21579189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12687442..12687442hg38UCSC Ensembl
chr9:12687442..12687442hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159756
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630884
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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