A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941090



Internal ID22716508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6097151..6097330hg38UCSC Ensembl
chr19:6097162..6097341hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392842
Samples
Known GenesRFX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941090
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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