A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873017



Internal ID22647959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84936736..84938489hg38UCSC Ensembl
chr16:84970342..84972095hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873017
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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