A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628462



Internal ID21576767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87891954..87891954hg38UCSC Ensembl
chr9:90506869..90506869hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163214
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628462
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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