A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054391



Internal ID19143610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91054518..91142020hg38UCSC Ensembl
Innerchr11:90787686..90875188hg19UCSC Ensembl
Innerchr11:90427334..90514836hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3887503
hg1987503
hg1887503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1252n100
Supporting Variantsnssv3710703
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)nsv1054391
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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