A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452053



Internal ID21109606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92843601..92855000hg38UCSC Ensembl
chr10:94603358..94614757hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192117
Samples
Known GenesEXOC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452053
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer