A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766636



Internal ID20542496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114949660..114949660hg38UCSC Ensembl
chr9:117711940..117711940hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766636
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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