A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737451



Internal ID20513412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2435590..2435647hg38UCSC Ensembl
chr16:2485591..2485648hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266446
Samples
Known GenesCCNF
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737451
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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