A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020289



Internal ID19109508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12382641..12418220hg38UCSC Ensembl
Innerchr8:12240150..12275729hg19UCSC Ensembl
Innerchr8:12284521..12320100hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3835580
hg1935580
hg1835580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7066n100
Supporting Variantsnssv3664824, nssv3664825
Samples
Known GenesDEFB109P1, FAM66A, FAM90A25P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020289
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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