A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039294



Internal ID19128513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3395247..3600393hg38UCSC Ensembl
Innerchr11:3416477..3621623hg19UCSC Ensembl
Innerchr11:3373053..3578199hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38205147
hg19205147
hg18205147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1017n100
Supporting Variantsnssv3706393
Samples
Known GenesLOC650368
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039294
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