A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877045



Internal ID22652008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:123161404..123352739hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38191336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877045
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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