A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489428



Internal ID266709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:153239957..153831743hg38UCSC Ensembl
chr7:152937042..153528828hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38591787
hg19591787
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv494n206
Supporting Variantsnssv17005864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489428
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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