A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934367



Internal ID22709692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66404581..66404650hg38UCSC Ensembl
chr16:66438484..66438553hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389524
Samples
Known GenesCDH5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934367
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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