A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959571



Internal ID22734593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40186282..40186282hg38UCSC Ensembl
chr4:40187902..40187902hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959571
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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