A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640923



Internal ID21589228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87331095..87331095hg38UCSC Ensembl
chr9:89946010..89946010hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162525
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640923
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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