A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264463



Internal ID20473681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17172041..17172041hg38UCSC Ensembl
chr5:17172150..17172150hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg381648
hg191648
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763450
Supporting Variants
Samples
Known GenesLOC285696
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264463
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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