A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046356



Internal ID18788887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3607607..3752985hg38UCSC Ensembl
Innerchr11:3628837..3774215hg19UCSC Ensembl
Innerchr11:3585413..3730791hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38145379
hg19145379
hg18145379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512877
Samples
Known GenesART1, ART5, CHRNA10, NUP98, TRPC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046356
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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