A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445940



Internal ID21103493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109038504..109184919hg38UCSC Ensembl
chr10:110798262..110944677hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38146416
hg19146416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977310
Samples
Known GenesRNU6-53P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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