A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041303



Internal ID19130522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101067588..101088705hg38UCSC Ensembl
Innerchr14:101533925..101555042hg19UCSC Ensembl
Innerchr14:100603678..100624795hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3821118
hg1921118
hg1821118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3533551
Samples
Known GenesMEG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041303
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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