A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845483



Internal ID22620418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35351404..35360949hg38UCSC Ensembl
chr6:35319181..35328726hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg389546
hg199546
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505337
Samples
Known GenesPPARD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845483
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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