A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946190



Internal ID22721677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57776911..57777860hg38UCSC Ensembl
chr16:57810823..57811772hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38950
hg19950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389543
Samples
Known GenesKIFC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946190
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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