A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090983



Internal ID22000216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97610159..97610159hg38UCSC Ensembl
chr10:99369916..99369916hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597057
Samples
Known GenesHOGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090983
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