A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106961



Internal ID22016195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9624549..9624549hg38UCSC Ensembl
chr20:9605196..9605196hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634178
Samples
Known GenesPAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106961
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