A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884476



Internal ID22659459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39068336..39074170hg38UCSC Ensembl
chr1:39534008..39539842hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg385835
hg195835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884476
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