A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450643



Internal ID21108196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118693254..119214513hg38UCSC Ensembl
chr10:120452766..120974025hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38521260
hg19521260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187332
Samples
Known GenesCACUL1, EIF3A, FAM45A, FAM45B, GRK5, NANOS1, PRDX3, SFXN4, SNORA19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450643
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