A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438225



Internal ID21095778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115866322..115908468hg38UCSC Ensembl
chr10:117625833..117667979hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3842147
hg1942147
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183087
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438225
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