A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764469



Internal ID16058425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1835294..1841679hg38UCSC Ensembl
Innerchr11:1856524..1862909hg19UCSC Ensembl
Innerchr11:1813100..1819485hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg386386
hg196386
hg186386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553052
Supporting Variants
Samples
Known GenesSYT8, TNNI2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764469
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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