A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101692



Internal ID22010925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19924108..19924108hg38UCSC Ensembl
chr20:19904752..19904752hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635024
Samples
Known GenesRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101692
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