A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432149



Internal ID21394151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81411939..81414353hg38UCSC Ensembl
chr14:81878283..81880697hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg382415
hg192415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv242n172
Supporting Variantsnssv15749025
SamplesMDQ045
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432149
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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