A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844458



Internal ID22619393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165463027..165477173hg38UCSC Ensembl
chr6:165876515..165890661hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3814147
hg1914147
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502974
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844458
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