A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050166



Internal ID19139385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:59334082..59443959hg38UCSC Ensembl
Innerchr14:59800800..59910677hg19UCSC Ensembl
Innerchr14:58870553..58980430hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38109878
hg19109878
hg18109878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713497
Samples
Known GenesDAAM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050166
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer