A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642555



Internal ID21590860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126605969..126605969hg38UCSC Ensembl
chr9:129368248..129368248hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159741
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642555
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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