A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874666



Internal ID22649620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41187500..41191782hg38UCSC Ensembl
chr19:41693405..41697687hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384283
hg194283
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874666
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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