A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285357



Internal ID20494575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168228174..168228174hg38UCSC Ensembl
chr5:167655179..167655179hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756842
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285357
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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