A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421884



Internal ID200945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156321025..156354439hg38UCSC Ensembl
chr1:156290816..156324230hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3833415
hg1933415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891286
Samples
Known GenesCCT3, TSACC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421884
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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