A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434087



Internal ID21396089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73109850..73112849hg38UCSC Ensembl
chr3:73159001..73162000hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748629, nssv15747393, nssv15753812, nssv15746110, nssv15747480, nssv15753266
SamplesNB12, NB10, BTQ055, BTQ016, MDQ025, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434087
Frequency
Sample Size15
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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