A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868124



Internal ID22643059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41865776..41866875hg38UCSC Ensembl
chr19:42369845..42370945hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381100
hg191101
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475967
Samples
Known GenesRPS19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868124
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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