A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901643



Internal ID22676795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114880175..114979511hg38UCSC Ensembl
chr4:115801331..115900667hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3899337
hg1999337
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421688
Samples
Known GenesNDST4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901643
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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