A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864810



Internal ID22639745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50569835..50571061hg38UCSC Ensembl
chr13:51143971..51145197hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864810
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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