A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748703



Internal ID21386297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147094849..147096848hg38UCSC Ensembl
chr4:148016001..148018000hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434216
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748703
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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