A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630069



Internal ID21578374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11068..11068hg38UCSC Ensembl
chr9:11068..11068hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153124
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630069
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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