A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472864



Internal ID250567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96466921..96536339hg38UCSC Ensembl
chr4:97388072..97457490hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3869419
hg1969419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472864
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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