A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094363



Internal ID21284304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41373732..41378722hg38UCSC Ensembl
Innerchr13:41947868..41952858hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg384991
hg194991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111481
Supporting Variants
Samplessample36
Known GenesNAA16
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094363
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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