A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552826



Internal ID15993549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:412626..431606hg38UCSC Ensembl
Innerchr11:412626..431606hg19UCSC Ensembl
Innerchr11:402626..421606hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3818981
hg1918981
hg1818981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763441
Samples
Known GenesANO9, SIGIRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552826
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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