A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876343



Internal ID22651303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58452293..58454914hg38UCSC Ensembl
chr19:58963660..58966281hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382622
hg192622
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479339
Samples
Known GenesZNF324B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876343
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