A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069748



Internal ID21978981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10980..10980hg38UCSC Ensembl
chr5:10980..10980hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069748
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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