A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531166



Internal ID18482761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73988645..74075786hg38UCSC Ensembl
Innerchr14:74455348..74542489hg19UCSC Ensembl
Innerchr14:73525101..73612242hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3887142
hg1987142
hg1887142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048009
Supporting Variants
Samples
Known GenesALDH6A1, CCDC176, ENTPD5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531166
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