A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484762



Internal ID262169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108645387..108645495hg38UCSC Ensembl
chr7:108285831..108285939hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484762
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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