A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046366



Internal ID19135585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90895661..90946288hg38UCSC Ensembl
Innerchr11:90628829..90679456hg19UCSC Ensembl
Innerchr11:90268477..90319104hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3850628
hg1950628
hg1850628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710701
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)nsv1046366
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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