A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531080



Internal ID18482675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64709653..64779463hg38UCSC Ensembl
Innerchr14:65176371..65246181hg19UCSC Ensembl
Innerchr14:64246124..64315934hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3869811
hg1969811
hg1869811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035833
Supporting Variants
Samples
Known GenesPLEKHG3, SPTB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531080
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