A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101338



Internal ID21280376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33792696..33799369hg38UCSC Ensembl
Innerchr19:34283601..34290274hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg386674
hg196674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111284
Supporting Variants
Samplessample296
Known GenesKCTD15
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101338
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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