A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426098



Internal ID205041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47041379..47060035hg38UCSC Ensembl
chr1:47507051..47525707hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3818657
hg1918657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902852
Samples
Known GenesCYP4X1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426098
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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