A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050866



Internal ID19140085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26655300..26963005hg38UCSC Ensembl
Innerchr14:27124506..27432211hg19UCSC Ensembl
Innerchr14:26194346..26502051hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38307706
hg19307706
hg18307706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528547
Samples
Known GenesMIR4307
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050866
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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