A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962661



Internal ID42413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14306162..14306162hg38UCSC Ensembl
chr5:14306271..14306271hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553344
Supporting Variants
Samples
Known GenesTRIO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962661
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007991


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