A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038227



Internal ID19127446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94418982..94441907hg38UCSC Ensembl
Innerchr14:94885319..94908244hg19UCSC Ensembl
Innerchr14:93955072..93977997hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3822926
hg1922926
hg1822926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1963n100
Supporting Variantsnssv3711382
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038227
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