A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901888



Internal ID22677041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146955385..146955438hg38UCSC Ensembl
chr4:147876537..147876590hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901888
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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