A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046479



Internal ID19135698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25112285..25275435hg38UCSC Ensembl
Innerchr11:25133831..25296981hg19UCSC Ensembl
Innerchr11:25090407..25253557hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38163151
hg19163151
hg18163151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1077n100
Supporting Variantsnssv3521499, nssv3503460, nssv3519223, nssv3512588, nssv3502814
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)nsv1046479
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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