A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045401



Internal ID19134620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96895663..96943720hg38UCSC Ensembl
Innerchr11:96766663..96814720hg19UCSC Ensembl
Innerchr11:96271873..96319930hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3848058
hg1948058
hg1848058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508200
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)nsv1045401
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