A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017836



Internal ID18760369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10734291..10946107hg38UCSC Ensembl
Innerchr8:10591801..10803617hg19UCSC Ensembl
Innerchr8:10629211..10841027hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38211817
hg19211817
hg18211817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7011n100
Supporting Variantsnssv3754235
Samples
Known GenesMIR1322, PINX1, XKR6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017836
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