A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736493



Internal ID20512442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69374626..69374679hg38UCSC Ensembl
chr16:69408529..69408582hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293810
Samples
Known GenesTERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736493
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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