A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080366



Internal ID21989599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72924967..72924967hg38UCSC Ensembl
chr6:73634690..73634690hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573888
Samples
Known GenesKCNQ5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080366
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer