A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861516



Internal ID22636451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77215466..77218503hg38UCSC Ensembl
chr9:79830382..79833419hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg383038
hg193038
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514338
Samples
Known GenesVPS13A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861516
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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