A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079800



Internal ID21989033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168755389..168755389hg38UCSC Ensembl
chr5:168182394..168182394hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574942
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079800
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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