A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919858



Internal ID22695081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129528349..129528664hg38UCSC Ensembl
chr10:131326613..131326928hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361001
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919858
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