A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149489



Internal ID15880210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28100578..28144861hg38UCSC Ensembl
Innerchr14:28569784..28614067hg19UCSC Ensembl
Innerchr14:27639535..27683818hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3844284
hg1944284
hg1844284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564151
Supporting Variants
SamplesNINDS_173
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149489
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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