A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947268



Internal ID22722770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66552261..66552315hg38UCSC Ensembl
chr16:66586164..66586218hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947268
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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