A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879111



Internal ID22654079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52233060..52235459hg38UCSC Ensembl
chr19:52736313..52738712hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477962, nssv17477961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879111
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