A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761946



Internal ID20537806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76836363..76836363hg38UCSC Ensembl
chr9:79451279..79451279hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285602
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761946
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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