A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902019



Internal ID6263946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64403004..64878265hg19UCSC Ensembl
Outerchr14:64395569..64882380hg19UCSC Ensembl
Innerchr14:63472757..63948018hg18UCSC Ensembl
Outerchr14:63465322..63952133hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1501752
SamplesSP51021
Known GenesESR2, MTHFD1, SYNE2, TEX21P
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902019
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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