A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041529



Internal ID19130748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42379035..42409934hg38UCSC Ensembl
Innerchr11:42400585..42431484hg19UCSC Ensembl
Innerchr11:42357161..42388060hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3830900
hg1930900
hg1830900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513153
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)nsv1041529
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