A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870460



Internal ID22645396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5633675..5637182hg38UCSC Ensembl
chr19:5633686..5637193hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383508
hg193508
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478761
Samples
Known GenesSAFB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870460
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