A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432088



Internal ID21394090
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 StatusM
Merged Variants
Supporting Variantsnssv15748495, nssv15753394
SamplesBTQ038, BTQ055
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432088
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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