A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449085



Internal ID227334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2772422..2779293hg38UCSC Ensembl
chr4:2774149..2781020hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg386872
hg196872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449085
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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