A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512877



Internal ID18464472
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 StatusS
Merged Variantsnsv1046356
Supporting Variants
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)nssv3512877
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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