A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109370



Internal ID21270328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:115975016..115979355hg38UCSC Ensembl
Innerchr1:116517637..116521976hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg384340
hg194340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112105
Supporting Variants
Samplessample149
Known GenesSLC22A15
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109370
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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