A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564496



Internal ID16351905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41141404..41199131hg38UCSC Ensembl
Innerchr14:41610607..41668334hg19UCSC Ensembl
Innerchr14:40680357..40738084hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3857728
hg1957728
hg1857728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n54
Supporting Variantsnssv826859, nssv826851, nssv826843, nssv826852, nssv826848, nssv826869, nssv826870, nssv826858, nssv826857, nssv826868, nssv826865, nssv826847, nssv826846, nssv826864, nssv826863, nssv826860, nssv826856, nssv826855, nssv826853, nssv826854, nssv826850, nssv826867, nssv826861, nssv826844, nssv826866, nssv826862, nssv826845, nssv826849
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564496
Frequency
Sample Size17421
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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