A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888674



Internal ID22663683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43665831..43824484hg38UCSC Ensembl
chr5:43665933..43824586hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38158654
hg19158654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420858
Samples
Known GenesNNT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888674
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer