A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3533557



Internal ID18485152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101513808..101603185hg38UCSC Ensembl
Innerchr14:101980145..102069522hg19UCSC Ensembl
Innerchr14:101049898..101139275hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3889378
hg1989378
hg1889378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040582
Supporting Variants
Samples
Known GenesDIO3, DIO3OS, MIR1247
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3533557
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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