A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069357



Internal ID21978590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107394166..107394166hg38UCSC Ensembl
chr5:106729867..106729867hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547077
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069357
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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