A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741918



Internal ID20517897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85855649..85856052hg38UCSC Ensembl
chr16:85889255..85889658hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741918
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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