A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871528



Internal ID22646466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50053940..50056975hg38UCSC Ensembl
chr19:50557197..50560232hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg383036
hg193036
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1069n209
Supporting Variantsnssv17477383, nssv17477384
Samples
Known GenesFLJ26850
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871528
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