A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733263



Internal ID20509191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62983803..62984053hg38UCSC Ensembl
chr16:63017707..63017957hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733263
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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