A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478820



Internal ID256367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99306761..99320226hg38UCSC Ensembl
chr7:98904384..98917849hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3813466
hg1913466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478820
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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