A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047449



Internal ID19136668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97262088..97477642hg38UCSC Ensembl
Innerchr11:97133088..97348642hg19UCSC Ensembl
Innerchr11:96638298..96853852hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38215555
hg19215555
hg18215555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518620
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)nsv1047449
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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