A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489533



Internal ID266808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131651003..131652843hg38UCSC Ensembl
chr7:131335762..131337602hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489533
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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