A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048799



Internal ID19138018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99074770..99096391hg38UCSC Ensembl
Innerchr11:98945500..98967121hg19UCSC Ensembl
Innerchr11:98450710..98472331hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3821622
hg1921622
hg1821622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518874
Samples
Known GenesCNTN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048799
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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