A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733752



Internal ID20509682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3469227..3469417hg38UCSC Ensembl
chr16:3519227..3519417hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260938
Samples
Known GenesNAA60
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733752
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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