A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867868



Internal ID22642803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13159312..13161311hg38UCSC Ensembl
chr19:13270126..13272125hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1013n209
Supporting Variantsnssv17479965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867868
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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