A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552857



Internal ID15993580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:557342..641191hg38UCSC Ensembl
Innerchr11:557342..641191hg19UCSC Ensembl
Innerchr11:547342..631191hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3883850
hg1983850
hg1883850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1523n54
Supporting Variantsnssv763553
Samples
Known GenesC11orf35, CDHR5, DRD4, IRF7, LOC143666, MIR210, MIR210HG, PHRF1, RASSF7, SCT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552857
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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