A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867583



Internal ID22642518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83789554..83850636hg38UCSC Ensembl
chr16:83823159..83884241hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3861083
hg1961083
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474045, nssv17479711
Samples
Known GenesCDH13, HSBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867583
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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