A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875861



Internal ID22650820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16443227..16450725hg38UCSC Ensembl
chr19:16554038..16561536hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387499
hg197499
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473291
Samples
Known GenesEPS15L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875861
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