A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074846



Internal ID21984079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167364103..167364103hg38UCSC Ensembl
chr5:166791108..166791108hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574123
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074846
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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