A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079078



Internal ID21988311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96516062..96516062hg38UCSC Ensembl
chr5:95851766..95851766hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38869
hg19869
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079078
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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