A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078824



Internal ID21988057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80465327..80465327hg38UCSC Ensembl
chr5:79761146..79761146hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg382479
hg192479
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539871
Samples
Known GenesZFYVE16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078824
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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