A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766219



Internal ID20542079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135847849..135847849hg38UCSC Ensembl
chr9:138739695..138739695hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274509
Samples
Known GenesCAMSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766219
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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