A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909086



Internal ID22684296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16761962..17211984hg38UCSC Ensembl
chr10:16803961..17253983hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38450023
hg19450023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362522
Samples
Known GenesCUBN, RSU1, TRDMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909086
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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