A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038990



Internal ID18781521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101824112..101946038hg38UCSC Ensembl
Innerchr14:102290449..102412375hg19UCSC Ensembl
Innerchr14:101360202..101482128hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38121927
hg19121927
hg18121927
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3533558
Samples
Known GenesPPP2R5C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038990
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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