A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762238



Internal ID20538098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67809180..67809180hg38UCSC Ensembl
chr16:67843083..67843083hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260572
Samples
Known GenesTSNAXIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762238
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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