A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033813



Internal ID19123034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8229622..8290767hg38UCSC Ensembl
Innerchr8:8087144..8148289hg19UCSC Ensembl
Innerchr8:8124554..8185699hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3861146
hg1961146
hg1861146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7002n100
Supporting Variantsnssv3681661, nssv3754224
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033813
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