A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464266



Internal ID242147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62944738..63355257hg38UCSC Ensembl
chr4:63810456..64220975hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38410520
hg19410520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16950241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464266
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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