A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031442



Internal ID19120664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46015453hg38UCSC Ensembl
Innerchr8:46847522..46927075hg19UCSC Ensembl
Innerchr8:46966687..47046240hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3879554
hg1979554
hg1879554
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7199n100
Supporting Variantsnssv3687366
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)nsv1031442
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