A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751387



Internal ID20527247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87867896..87867896hg38UCSC Ensembl
chr9:90482811..90482811hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751387
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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