A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866703



Internal ID22641638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32413176..32414775hg38UCSC Ensembl
chr13:32987313..32988912hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452824
Samples
Known GenesN4BP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866703
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