A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856336



Internal ID22631271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41950662..41952061hg38UCSC Ensembl
chr14:42419865..42421264hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459768, nssv17467429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856336
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