A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870747



Internal ID22645683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33204816..33216797hg38UCSC Ensembl
chr19:33695722..33707703hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3811982
hg1911982
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474701
Samples
Known GenesLRP3, SLC7A10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870747
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