A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872016



Internal ID22646954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12961802..12968770hg38UCSC Ensembl
chr19:13072616..13079584hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386969
hg196969
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872016
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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