A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047116



Internal ID19136335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90650007..90677437hg38UCSC Ensembl
Innerchr11:90383175..90410605hg19UCSC Ensembl
Innerchr11:90022823..90050253hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3827431
hg1927431
hg1827431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710700
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047116
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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