A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767145



Internal ID20543005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108000375..108000375hg38UCSC Ensembl
chr9:110762656..110762656hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767145
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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