A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934827



Internal ID22710159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57773848..57773971hg38UCSC Ensembl
chr16:57807760..57807883hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387044
Samples
Known GenesKIFC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934827
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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