A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660330



Internal ID15396982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20052901..20093921hg38UCSC Ensembl
Innerchr14:20521060..20562080hg19UCSC Ensembl
Innerchr14:19590900..19631920hg18UCSC Ensembl
Innerchr14:19590900..19631920hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3841021
hg1941021
hg1841021
hg1741021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520054
Supporting Variants
Samples
Known GenesOR4L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660330
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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