A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036884



Internal ID19126103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93868880..93887534hg38UCSC Ensembl
Innerchr14:94335226..94353880hg19UCSC Ensembl
Innerchr14:93404979..93423633hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3818655
hg1918655
hg1818655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532598
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)nsv1036884
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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