A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069666



Internal ID21978899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2099083..2099083hg38UCSC Ensembl
chr5:2099197..2099197hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069666
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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