A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287489



Internal ID20496707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173891182..173891182hg38UCSC Ensembl
chr5:173318185..173318185hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756009
Supporting Variants
Samples
Known GenesCPEB4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287489
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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