A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268430



Internal ID20477648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158440304..158440304hg38UCSC Ensembl
chr5:157867312..157867312hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg384846
hg194846
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268430
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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