A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036863



Internal ID19126082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99888859..99950711hg38UCSC Ensembl
Innerchr14:100355196..100417048hg19UCSC Ensembl
Innerchr14:99424949..99486801hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3861853
hg1961853
hg1861853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3533447
Samples
Known GenesEML1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036863
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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