A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096203



Internal ID21271686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31726748..32223622hg38UCSC Ensembl
Innerchr15:32018951..32515823hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38496875
hg19496873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116680
Supporting Variants
Samplessample167
Known GenesCHRNA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096203
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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