A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050436



Internal ID19139655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82051974..82140003hg38UCSC Ensembl
Innerchr14:82518318..82606347hg19UCSC Ensembl
Innerchr14:81588071..81676100hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3888030
hg1988030
hg1888030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531230
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)nsv1050436
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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