A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528569



Internal ID18826850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27567831..27632285hg38UCSC Ensembl
Innerchr14:28037037..28101491hg19UCSC Ensembl
Innerchr14:27106877..27171331hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3864455
hg1964455
hg1864455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052216
Supporting Variants
Samples
Known GenesLINC00645
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3528569
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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