A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850883



Internal ID22625818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54581238..54584183hg38UCSC Ensembl
chr15:54873436..54876381hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382946
hg192946
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472897
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850883
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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