A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766671



Internal ID20542531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32906851..32906851hg38UCSC Ensembl
chr9:32906849..32906849hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766671
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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