A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041477



Internal ID19130696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81573720..81589607hg38UCSC Ensembl
Innerchr11:81284762..81300649hg19UCSC Ensembl
Innerchr11:80962410..80978297hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3815888
hg1915888
hg1815888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513083
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)nsv1041477
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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