A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15754458



Internal ID21388217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81411868..81414268hg38UCSC Ensembl
chr14:81878212..81880612hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg382401
hg192401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432148
Supporting Variants
SamplesNB07
Known GenesSTON2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15754458
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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