A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873109



Internal ID22648053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83661856..83664355hg38UCSC Ensembl
chr16:83695461..83697960hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474042
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873109
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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