A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896702



Internal ID22671797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151632518..151659307hg38UCSC Ensembl
chr4:152553670..152580459hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3826790
hg1926790
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427924
Samples
Known GenesFAM160A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896702
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