A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519095



Internal ID15446388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33133754..33176816hg38UCSC Ensembl
Innerchr14:33602960..33646022hg19UCSC Ensembl
Innerchr14:32672711..32715773hg18UCSC Ensembl
Innerchr14:32672711..32715773hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3843063
hg1943063
hg1843063
hg1743063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696569
Samples
Known GenesNPAS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519095
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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