A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964909



Internal ID43918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51400121..51400136hg38UCSC Ensembl
chr5:50695955..50695970hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964909
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.105912


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