A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053196



Internal ID19142415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90500367..90644031hg38UCSC Ensembl
Innerchr11:90233535..90377199hg19UCSC Ensembl
Innerchr11:89873183..90016847hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38143665
hg19143665
hg18143665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521624
Samples
Known GenesDISC1FP1, MIR4490
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053196
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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