A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637611



Internal ID21585916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32463888..32463888hg38UCSC Ensembl
chr9:32463886..32463886hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161602
SamplesHG00731
Known GenesDDX58
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637611
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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