A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711406



Internal ID18663001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105612353..105813104hg38UCSC Ensembl
Innerchr14:106078690..106279432hg19UCSC Ensembl
Innerchr14:105149735..105350477hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38200752
hg19200743
hg18200743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050098
Supporting Variants
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3711406
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