A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765460



Internal ID20541320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94491149..94491149hg38UCSC Ensembl
chr8:95503377..95503377hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266877
Samples
Known GenesKIAA1429
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765460
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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