A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036936



Internal ID19126155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:69537889..69556215hg38UCSC Ensembl
Innerchr14:70004606..70022932hg19UCSC Ensembl
Innerchr14:69074359..69092685hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3818327
hg1918327
hg1818327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531115
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)nsv1036936
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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