A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095367



Internal ID21269818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:29698914..29701891hg38UCSC Ensembl
Innerchr14:30168120..30171097hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382978
hg192978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110438
Supporting Variants
Samplessample143
Known GenesMIR548AI, PRKD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095367
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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