A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097766



Internal ID22006999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110360402..110360402hg38UCSC Ensembl
chr10:112120160..112120160hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097766
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