A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553140



Internal ID16340549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3546814..3639684hg38UCSC Ensembl
Innerchr11:3568044..3660914hg19UCSC Ensembl
Innerchr11:3524620..3617490hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3892871
hg1992871
hg1892871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174288
SamplesHGDP00108
Known GenesART5, TRPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553140
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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