A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880959



Internal ID22655930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61876358..61880322hg38UCSC Ensembl
chr16:61910262..61914226hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383965
hg193965
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472189
Samples
Known GenesCDH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880959
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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