A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447019



Internal ID225333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:195437877..195497091hg38UCSC Ensembl
chr1:195407007..195466221hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3859215
hg1959215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16894533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447019
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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