A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882867



Internal ID22657844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35817765..35818797hg38UCSC Ensembl
chr19:36308667..36309699hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381033
hg191033
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882867
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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