A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085785



Internal ID21995018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102628854..102628854hg38UCSC Ensembl
chr10:104388611..104388611hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582664
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085785
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