A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039820



Internal ID19129039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44828809..44892206hg38UCSC Ensembl
Innerchr14:45298012..45361409hg19UCSC Ensembl
Innerchr14:44367762..44431159hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3863398
hg1963398
hg1863398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530437
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039820
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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