A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15753394



Internal ID21385268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33184198..33209303hg38UCSC Ensembl
chr14:33653404..33678509hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3825106
hg1925106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432088
Supporting Variants
SamplesBTQ055
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15753394
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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