A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432087



Internal ID21394089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32938477..32939623hg38UCSC Ensembl
chr14:33407683..33408829hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381147
hg191147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747363
SamplesNB08
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432087
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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