A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089455



Internal ID21998688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61998092..61998092hg38UCSC Ensembl
chr10:63757851..63757851hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580357
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089455
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